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Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position Summary :- Manage transactional data operational challenges affecting BMS sites, CMOs and 3PLs. Lead effort to analyze and mitigate transactional data challenges by market. Support managing initiatives to develop a digitization strategy to enable faster and effective decision-making. SME in transactionaldata management, support data work stream for various supply chain compliance implementations, as well as provide ongoing continuous improvement support to sustain the transaction regulatory requirements globally. Support data work stream during various business development activities, such as divestures, acquisitions, new product launch &amp; product life cycles to support business units Responsibilities :-Support and maintain transactional data operations workstream. Assure overall transactional data operations objectives are achieved (e.g., right first time). Build and maintain strong relationships with stakeholders across functional areas (e.g., Logistics, O2C, Master Data and Packaging for internal / external, Quality, IT). Ensure full consideration of transaction related data requirements across functional areas. Responsible for maintaining technical solutions to ensure timely compliance with all market transaction regulatory requirements. Champion data work stream collaboration with partners for existing and new product introduction. Perform analysis and recommend mitigation strategies to teams in support of partnerships; collaborate to ensure sound decisions; assure projects remain on track and CAPAs are closed on time. Support commercial change management process for transactional data operations. Project or market dependent, may be the impact assessor. Perform transaction data operation assessments stemming from CAPA. Manage daily transactional data operational issues for commercial products. Develop transaction operational capabilities to ensure efficiency, robustness, and sustainability. Reports dashboard metrics, transactional data by lot, site, and markets. Manages technical assessment arising from Quality alert event. Monitor the sustainability of the technical processes already implemented. Support remediation of process to assure proper and accurate process flow of transactional data based on physical product flow. Propose process improvements and support implementation / execution to mitigate gaps and approve overall process robustness. Assures standard process for the implementation of transactional data capabilities and recommends process improvements at sites, CMOs and or 3PLs ensuring timely delivery, efficiency, robustness, and sustainability.Required Competencies :- Demonstrated excellent organizational skills and attention to detail. Demonstrated flexibility and capability of managing multiple assignments, excellent oral and written communication skills, and computer competence. Self-direction with the ability to take initiative and manage deadlines and stakeholders is required. Ability to create effective change in a team based collaborative environment. Ability to work in a fast-paced environment, organized and able to prioritize tasks to meet multiple deadlines.Required Qualifications and desired experience:- BA or BS degree in Business, supply chain management or equivalent 5 - 7 years total business experience, pharmaceutical, serialization and/or supply chain logistics, Order to Cash experience with at least 2 yrs. in data or data operation related area. Solid understanding of key relationships, dependencies, and interfaces among business units, IT, and external partners. Experience in SAP or similar traceability ERP systemsIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Manager, Transaction Data Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.The Technician Specialist Bulk Operations will be responsible for manufacturing products (capsules and tablets) in compliance with GMP / cGMP regulations, health and safety rules. He/she will have to comply with the procedures defined by the pharmaceutical site's quality system.The technician specialist will be also responsible for providing technical support to operators in production activities, update/create technical documentation as well as being the SME in projects.Duties/Responsibilities <ul><li>Carry out production operations such as raw materials weighing, powder mixing and operating the various production lines for both the capsule and tablet manufacturing processes in accordance with quality system procedures.</li><li>Carry out equipment, materials and rooms cleaning involved according to production activities.</li><li>Carry out In Process Control, format changes, line clearance of the production line and manufacturing batch review.</li><li>Check, record and complete the pre-established working documents to monitor the operations carried out (batch records completed in accordance with GMP).</li><li>Provide technical support to operators in production activities and act as Technical Trainer.</li><li>Act as technical SME in various projects, help to fix line breakdown, understand how machines work, use problem solving tools.</li><li>Master the ERP and MES tools in the management of batch records and associated consumption.</li><li>Update/create technical documentation.</li><li>Participate in and support qualification/validation activities.</li><li>Participate in continuous improvement by proposing ideas for improvements and promoting LEAN within the team</li></ul>Qualifications<ul><li>CFC level and ideally 8 years' experience or 4 years' experience as a technician in the pharmaceutical industry.</li><li>Have good knowledge of GMP environment and pharmaceutical industry.</li><li>Have a good knowledge in the areas of oral drug processing techniques such as dry formulation, encapsulation, powder compression and other wet/dry granulation.</li><li>Fluent in French and a good understanding of English (level B1).</li><li>Be versatile, organized and rigorous, with excellent interpersonal skills for teamwork.</li><li>Be a critical thinker and a source of ideas to continuously improve the way of working (Yellow Belt certification).</li><li>Very good knowledge of IT tools (Word, Excel, Powerpoint, Outlook) and MES / ERP.</li></ul>.&nbsp;If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Technician specialiste Bulk Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Bristol Myers Squibb IrelandBristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, haematology, immunology, cardiovascular and neuroscience. Our employees work every day to transform patients’ lives through science.Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. Many of the global business services, including the European Treasury Centre, Market Supply Operations and Commercial Operations have a presence in Ireland.&nbsp;Ireland is also home to External manufacturing’s global headquarters, the business unit responsible for the management of manufacturing contract operations (CMO’s) and ensuring reliable supply of product to patients across the Bristol Myers Squibb global network.Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility.&nbsp; This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.For more information about Bristol Myers Squibb, visit us at BMS.com/ieThe RoleThe Regulatory Operations Manager is responsible for all regulatory support activities within External Manufacturing to ensure that the manufacture of products by Contract Manufacturing Organizations (CMOs) is aligned with the appropriate regulatory dossiers.Key Duties and Responsibilities:<ul><li>Develop and manage appropriate business processes to support Regulatory Dossier Management for products supported by External Manufacturing</li><li>Manage the notification of Change Control approvals and regulatory renewals to CMOs as appropriate, to ensure that the CMO has the most up-to-date regulatory dossiers</li><li>Manage a process to ensure appropriate batch restrictions are applied in the case of change controls where regulatory approvals are required</li><li>Manage regulatory documentation requests to support filings, updates, annual reports renewals and Health Authority (HA) requests</li><li>Review relevant Chemistry, Manufacturing and Controls (CMC) sections of new drug applications (NDA’s) and market authorisation applications (MAAs) and provide support for filings</li><li>Provide Good Manufacturing Practice (GMP) and Regulatory training as required</li></ul><ul><li>Participating in other Quality Assurance (QA) supporting activities as required (e.g. internal audits, site regulatory inspections, Annual Product Quality Reviews (APQR’s), quality risk management).</li><li>Manage the follow-up and close out of regulatory actions associated with External Manufacturing (ExM) Change Controls</li></ul>What’s important to usEmployees are expected to display the BMS Values, which move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases:<ul><li>Passion: Our dedication to learning and excellence helps us to deliver exceptional results. </li><li>Innovation: We pursue disruptive and bold solutions for patients. </li><li>Urgency: We move together with speed and quality because patients are waiting.</li><li>Accountability: We all own BMS’ success and strive to be transparent and deliver on our commitments.</li><li>Integrity: We demonstrate ethics, integrity and quality in everything we do for patients, customers and colleagues.</li><li>Inclusion: We embrace diversity and foster an environment where we can all work together at our full potential. </li></ul>We have a passion for tackling the toughest diseases, which inspires innovation and speed in our daily work and a sense of accountability to the patients we serve.Why you should apply<ul><li>You will help patients in their fight against serious diseases</li><li>You will&nbsp;be part of&nbsp;a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.</li><li>You’ll get a competitive salary and a great benefits package</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Manager Regulatory Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.SUMMARY:The Associate Director of Incident Response will be responsible for assisting and actioning Cyber Incident Response within the BMS Cyber Fusion Center (CFC). This role is responsible for responding to alerts and incidents within the BMS enterprise and to aid in providing technical guidance to team members. The ideal candidate will be highly technical, with an ability to quickly provide leadership level summaries while potentially dealing with multiple incidents. This role may also require the candidate to provide support as an incident commander, if the need arises.&nbsp;POSITION RESPONSIBILITIES:<ul><li>Investigate and lead incident response incidents and investigations, end-to-end&nbsp;</li><li>Leverage EDR tools to investigate and identify malicious activity to determine root cause&nbsp;</li><li>Supporting IR investigations by using malware, log, and network analysis&nbsp;</li><li>Conducting some threat hunting to support investigations&nbsp;</li><li>Working in Cloud platforms to conduct investigations&nbsp;</li><li>Working with threat intelligence to identify tools, tactics, and procedures (TTP) and indicators of compromise (IOC)&nbsp;</li><li>Providing expert opinion and insight into cyber related matters affecting BMS&nbsp;</li><li>Creating comprehensive analysis reports and potential after action reports, as needed&nbsp;</li><li>Communicating concisely and effectively with internal BMS stakeholders&nbsp;</li><li>Support CFC leadership on cyber related issues&nbsp;</li><li>Assist development of SOP’s and other necessary documentation for the CFC&nbsp;&nbsp;</li></ul>DESIRED EXPERIENCE:<ul><li>At least 5 years of hand on experience in Incident Response&nbsp;&nbsp;</li><li>At least 3 years of experience with SIEM, such as Sentinel or Splunk&nbsp;&nbsp;</li><li>After hours escalation and on-call responsibilities can be expected&nbsp;</li><li>MITRE ATT&amp;CK framework knowledge&nbsp;</li><li>Prior blue team IR exposure and analysis&nbsp;</li><li>Demonstrated SIEM platform alert analysis experience.&nbsp;</li><li>Expert-level knowledge of common attack vectors and penetration techniques.&nbsp;</li><li>Solid working knowledge of networking technology and tools, firewalls, proxies, IDS/IPS, encryption.&nbsp;</li><li>Technical writing and presentation skills.&nbsp;</li><li>Event analysis and correlation.&nbsp;</li><li>Experience with Linux (CLI), MAC OSX, and Windows operating systems&nbsp;</li><li>Experience with cloud elements (S3, Impala, Athena, etc)&nbsp;</li></ul> Ideal Candidates Would Also Have:&nbsp;<ul><li>Certified in one or more of the following: SANS 500 level course (GCIA, GCIH, etc)&nbsp;</li><li>Strong understanding of networking fundamentals (routing, OSI layers, CIDR).&nbsp;</li><li>Experience in fast-paced environment.&nbsp;&nbsp;&nbsp;</li><li>Experience with programming or scripting languages (Python, bash).&nbsp;</li><li>Ability to present highly technical information to non-technical audiences&nbsp;</li><li>Solid understanding of sigma rules and their creation&nbsp;</li><li>A working understanding of ATC RE&amp;CT and VERIS</li></ul>The starting compensation for this job&nbsp;is a range from $156,000 - $195,000 plus incentive cash and stock opportunities (based on eligibility). &nbsp;The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided&nbsp;based on demonstrated&nbsp;experience.&nbsp;Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit <a href="https://careers.bms.com/life-at-bms/" target="_blank">https://careers.bms.com/life-at-bms/</a>.Benefit&nbsp;offerings&nbsp;are subject to the terms and conditions of the applicable plans then in effect&nbsp;and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support&nbsp;such as&nbsp;the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.&nbsp;Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.&nbsp;Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate Director, Incident Response, Cybersecurity Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe Digital Manufacturing EMES team, part of BMS’ Global Manufacturing IT organization, is seeking a Computer System Validation Lead to meet evolving and growing needs for IT/Compliance across the company’s manufacturing operations. The successful candidate will apply their compliance/validation skills for the validation of Manufacturing Execution System (Syncade) to directly support BMS’ worldwide manufacturing operations.If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!Key Responsibilities<ul><li>Develop and implement the test automation strategy, ensuring alignment with overall project goals and timelines. Design, develop, and maintain automated test scripts using industry-standard tools and frameworks.</li><li>Ensure comprehensive test coverage by identifying and automating test cases for functional, regression, performance, and load testing. Continuously improve and optimize the test automation framework and processes.</li><li>Conduct code reviews and provide feedback to ensure the quality and maintainability of automated test scripts. Monitor and analyse test results, identifying and reporting defects, and working with development teams to resolve issues. Ensure that automated tests are integrated into the continuous integration/continuous deployment (CI/CD) pipeline.</li><li>Collaborate with cross-functional teams, including developers, product managers, and QA engineers, to define and prioritize automation testing requirements.</li><li>Create and maintain detailed documentation for test automation processes, frameworks, and scripts. Generate and present test reports, metrics, and dashboards to stakeholders, providing insights into the quality and stability of the software.</li><li>Stay up-to-date with the latest trends and best practices in test automation and quality assurance. Identify opportunities for process improvements and implement changes to enhance the efficiency and effectiveness of the testing process. Provide training and support to team members and other stakeholders on test automation tools and practices.</li><li>Develop and review of Computer System Validation Artifacts including Validation Master plans, Requirements Specification, Design Specifications, Test Plans (System Test, User Acceptance Test, Installation Qualification), Test Summary Reports (System Test, User Acceptance Test, Installation Qualification), Traceability Matrix, Validation Summary Report, Release for Use Memo, SOP's, Work Instructions.</li><li>Develops complete understanding of BMS policies and procedures related to all aspects of computer system validation. Ensure that the validation artifacts meet the quality requirements and applicable regulations FDA, EU, Corporate &amp; International Standards.</li><li>Collaborate with Validation Cross Functional Teams at corporate and related to management, peers and junior professionals. Lead the team in preparation for regulatory, internal, and corporate audits and inspections.</li></ul>Qualifications &amp; Experience<ul><li>The Test Lead should hold a minimum of a BS qualification (Degree) in a scientific, technical, or engineering discipline along with 10+ years’ of experience in software testing and test automation, with at least 2 years in a leadership or senior role.</li><li>Good technical understanding of IT Infrastructure, manufacturing execution systems and its integration with process automation systems (DeltaV), LIMS (Labware), SAP/Oracle is desirable.</li><li>Knowledge of Automation testing tools (e.g., Selenium, QTP, Appium). Strong understanding of test automation frameworks (e.g., TestNG, JUnit).</li><li>Strong Knowledge of programming languages (e.g., Java, Python, C#) .</li><li>Experience with CI/CD tools (e.g., Jenkins, Bamboo). Understanding of the integration of testing processes within CI/CD pipelines.</li><li>Knowledge of FDA regulatory validation requirements including FDA (21CFR, part 11), EMA (Annex 11), GAMP and all other Worldwide Regulatory requirements (ICH Q7, Q8, Q9). Relevant experience with data integrity requirements and implementation in a GMP environment.</li><li>Knowledge of Quality principles, computer system development lifecycles, QA methodologies, S88 batch control standards and the and ISA-95 manufacturing plant levels.</li><li>Problem solving ability, Critical thinking, and ability to effectively communicate with technical and non-technical stakeholders.</li><li>Strong service delivery, time, project, and priority management skills.</li><li>Experience dealing with regulatory agencies and global audit teams is desirable.</li></ul>#HYDIT #LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Testing Strategy and Automation Lead  – Digital Manufacturing

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Working With UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-usWorking with Us Challenging. Meaningful. Life-changing. Those are not words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You will get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us Position SummaryProvide Quality assistance and oversight to operations, for in-process intermediates and manufactured products, and other GMP processes as required. Performs review and approval of documentation associated with in-process materials, and manufactured product. Assists in the identification, generation and quality review of investigation records that may result during day-to-day operations. Assure the quality of manufactured products complies with all applicable regulations and guidelines.&nbsp; This position is Monday- Friday First Shift Schedule with the hours of 07:00 am - 03:30 pm.Key Responsibilities<ul><li>Quality floor support of complex manufacturing activities</li><li>Performs manufacturing batch production record review in support of product release in accordance with specifications and SOPs.</li><li>Perform walkthroughs of GMP areas documenting observations and areas of concern.&nbsp;</li><li>Perform training on routine facility Quality tasks for new team members.</li><li>Supports return to service walkthroughs and Manufacturing inspection readiness walkthroughs per procedures as needed.</li><li>Assures all electronic and paper documentation, which requires QA review is in compliance with corporate and site procedures, cGMP regulations, and other industry guidelines.</li><li>May support review of quality master data.</li><li>Authors and revises Quality specific SOPs and may provide Quality review and approval of manufacturing related SOPs.&nbsp;</li><li>May provide guidance to less experienced staff.</li><li>Support the Quality approval of Master Batch Records or Syncade Recipes.</li><li>Supports the Quality review and closure of no impact manufacturing deviations.</li><li>May support release of incoming or manufactured products.</li><li>Routine QA Floor Support Activities, including alarm review, logbook review, etc.</li><li>Other duties as assigned.</li></ul>Qualifications &amp; Experience <ul><li>Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent is preferred.</li><li>A minimum of 4 years of relevant experience in a regulated environment with 2 years focused on quality preferred.</li><li>Knowledge of biotech bulk and finished product manufacturing, analytical testing is highly desirable.</li><li>Knowledge of US and EU cGMP regulations and guidance.&nbsp;</li><li>Knowledge of electronic or paper batch record systems, DeltaV, and other electronic systems applicable to laboratory test result generation, inventory management, investigations and equipment tracking and maintenance is desirable.</li></ul>This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.If you come across a role that intrigues you but does not perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™,” every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues.On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. ￼BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodation/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.&nbsp;BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.LocationsDevens - MA - USCompensation GradeEG-090On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Field Quality, QA Operations Senior Specialist (07:00 am - 03:30 pm)

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science.&nbsp;In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.<h4>Position: Manufacturing Operations, Senior Team Leader (3rd shift)</h4><h4>Location: Humacao - PR</h4>Key Responsibilities<ul><li>Leads a Manufacturing Production area Team to ensure that production, competitive cost, quality/regulatory, customer service requirements are met or exceeded.</li><li>&nbsp;Plans and organizes the area work to achieve a High Performing Team environment.&nbsp; Manages the assigned operations area people staffing, performance assessment, merit increase /annual performance bonus, counseling/coaching/disciplinary &amp; corrective actions, and takes action for performance improvement as well as career development.</li><li>Ensures that work performed by area team members is accurate, timely, efficient and compliant with corporate policies, SOPs, cGMP regulations, and regulatory agencies regulations (FDA, EMEA). Assures a streamlined and continuous process flow of Manufacturing Operations area. Monitors, evaluates and communicates area performance metrics for processes, cost and quality. Determines production schedule, updates schedule’s board, communicates daily schedule performance to team members and communicates the shift production information with other shifts leaders. Reduces cycle times and optimizes production scheduling by the use of innovation tools including.</li><li>Ensures the application of cGMP compliance with respect to the Team, shop floor and documentation.&nbsp;&nbsp;</li><li>Trains the Team on any necessary compliance and quality requirements related with the area or the business. Reviews Batch Records (Paper/Electronic) and manages discrepancies.</li><li>Collaborates effectively with other functional SMEs to ensure production goals are met and investigations are expeditiously completed. Participates in and may lead continuous improvement initiatives applying tools like: 5S, LEAN manufacturing and Six Sigma to improve quality, cost, safety and cycle time. Performs administrative duties for the assigned area that include team members attendance monitoring, attendance timecards approval, vacations scheduling and approval and overtime coordination to meet production requirements.</li><li>Provides, in coordination with other departments, the guidance and resources to support technology transfer activities, equipment qualification, process validation, troubleshooting, clinical lots production, and process optimization.</li><li>Participates in quality and safety investigations. Provides support to the regulatory affair reports, customer complaints, and area exception reports (e.g., Quality Investigation Reports, Quality Complimentary Reports, Change Request Forms, etc.).</li><li>Ensures that area Team members comply with the established learning curriculum to achieve proper knowledge transfer/acquisition. Participates actively as a key contact member of the OSD operations areas in the internal and external audits.</li><li>&nbsp;Provides input in the creation and revision of SOP’s, protocols, batch records and related documents to assure compliance with cGMP’s, company policies / procedures and documentation practices. Maintains control of all environmental/safety issues in the OSD Manufacturing operation areas. Serves as the back-up of the OSD Operations Manufacturing Manager, as requested.</li><li>&nbsp;Maintains accurate tracking records and provides timely feedback to Manager regarding status of costs in the assigned area relating to overtime and waste.&nbsp;</li><li>&nbsp;Monitors usage and expenses related to supplies and labor costs in the work area.&nbsp; Implements shop floor continuous improvement practices to meet financial standards. Promotes and models the BMS Core Behaviors, facilitating teamwork, providing coaching and feedback.</li></ul>Qualifications &amp; Experience<ul><li>BS&nbsp; Degree&nbsp; in&nbsp; Engineering&nbsp; /Biology/&nbsp; Chemistry,&nbsp; Pharmacy&nbsp; or&nbsp; related&nbsp; sciences&nbsp; with&nbsp; three&nbsp; (3)&nbsp; years&nbsp; of&nbsp; experience&nbsp; in pharmaceutical&nbsp; OSD&nbsp; manufacturing&nbsp; processes;&nbsp; or&nbsp; BBA&nbsp; Degree&nbsp; in&nbsp; Business&nbsp; Administration&nbsp; with&nbsp; five&nbsp; (5)&nbsp; years&nbsp; of experience in pharmaceutical OSD manufacturing processes.</li><li>&nbsp;Proven in-depth technical knowledge on Oral Solid Dosage Manufacturing processes•Proficient in regulatory / compliance areas of cGMPs, FDA regulations, EHS.</li><li>Basic understanding of product cost structure, budgeting process and spending.</li><li>Three (3) years of experience in a supervisory / managerial position.</li><li>One&nbsp; (1)&nbsp; year&nbsp; experience&nbsp; in&nbsp; a&nbsp; very&nbsp; highly&nbsp; automated&nbsp; manufacturing&nbsp; operations&nbsp; environment&nbsp; (Electronic&nbsp; Batch Records/NIR-PAT Technology).</li><li>Proven strong leadership skills managing performance to the attainment of high performing team •Knowledge and experience implementing Six Sigma and Lean Manufacturing.</li><li>Strong business sense.</li><li>Sense of urgency, accountability and agile decision making.</li><li>Understanding of and capability to support financial and total quality/safety objectives.</li><li>Assertiveness and uncompromising attitude with regard to the quality standardsThis is a list —­ style: List Paragraph.</li></ul>Working Conditions<ul><li>Exposed to various working environments which may potentially expose the incumbent, for which protective equipment is required.</li><li>Some travel required to attend meetings and trainings.</li></ul>BMSBLAround the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.&nbsp;Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation.&nbsp; Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment.&nbsp; This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

OSD Manufacturing Operations, Senior Team Leader (3rd shift)

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.RayzeBio is seeking a Director of Quality Operations at our state-of-the-art Radiopharmaceutical Manufacturing Facility in Indianapolis, IN (USA). &nbsp;This role will be responsible for overseeing all Quality aspects related to GMP production of Isotopes and the RayzeBio pipeline of radiopharmaceutical drug products for global clinical trial and commercial use. This role will partner with external and internal stakeholders driving Quality Systems at the Indianapolis site. &nbsp;The Director of Quality Operations will drive a culture of Quality and ensure GMP compliance and the successful and timely execution of day-to-day production operations supporting global distribution of isotope and drug products.&nbsp; Additional responsibilities include establishing and managing Quality Operational KPI’s, supporting and driving operational improvements within the Quality organization. &nbsp;The Director of Quality Operations will support the sites transition for clinical to commercial operations and be a key Quality leader supporting operational readiness for QP, PAI and other Regulatory Authority quality audits. This role will drive a site culture of Quality with a patient first mindset. Key Responsibilities:Essential duties and responsibilities include the following. &nbsp;Other duties may be assigned.<ul><li>Responsible for Quality Operations oversight and day-to-day Quality management related to isotope and Radiopharmaceutical drug product manufacturing at the Indianapolis facility.</li><li>&nbsp;Ensure adherence to applicable GMP regulations and company policies and procedures.</li><li>Collaborate with other business leaders across the organization to support the development, continuous improvement and lifecycle management of GMP policies and procedures.</li><li>&nbsp;Provide leadership and build an exceptional Quality Operations team.</li><li>Champion and foster a positive and quality compliant culture with a patient safety mindset.</li><li>Lead the implementation of site readiness for FDA Pre-Approval Inspection Pre-license inspection.&nbsp;</li><li>Support compliance audits and regulatory inspections by competent regulatory authority (e.g., FDA, EMA, PMDA, etc.).&nbsp;</li><li>Establish and manage Quality Operational KPI’s and related metrics.</li><li>Work collaboratively with Leads from Facilities and Engineering, Manufacturing, IT, Clinical Operations, Logistics, and MS&amp;T, to ensure the ongoing qualified and operational readiness for commercial manufacturing at the facility.</li><li>Support the implementation of corporate initiatives and ensure success toward annual corporate goals and objectives.</li></ul>Education and Experience:<ul><li>BS/MS in relevant Science or Engineering discipline and 10+ years of experience in building, managing and leading Quality Operations teams</li><li>Proven expertise in GMP operations and compliance for global clinical trial and commercial injectable or radiopharmaceutical operations required.</li><li>Strong background in US/EU regulations with regulatory agency inspection experience required.</li><li>Experience implementing and improving GMP Quality systems related to commercial manufacturing operations is required</li><li>Demonstrated Quality leadership through a partnership approach with manufacturing and other Quality teams to enable high quality and compliant product distribution to patients is required</li><li>Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships&nbsp;</li><li>Demonstrated excellence in written and verbal communication&nbsp;</li><li>Previous experience in a commercial GMP parenteral facility, previous Radiopharma experience a plus</li></ul>Skills and Qualifications:Beyond having the requisite experience and qualifications, a successful candidate will have a proven history of team and personnel leadership with high levels of self-motivation, adaptability, critical thinking, analysis, and creative problem-solving. This is a fast-paced position within a fast-paced organization, so the ability to come in and hit the ground running is critical for success in the role.&nbsp;#LI-ONSITE #RayzebioIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Associate Director/Director, Quality Operations, Radiopharmaceutical Manufacturing

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Key ResponsibilitiesResponsibilities include but are not limited to:&nbsp;<ul><li>Execute routine Bioburden, Endotoxin, and Microbial Identification testing in accordance with SOPs, safety, and cGMP guidelines to support the release and stability of finished products, raw materials, in-process materials, and various components.&nbsp;</li><li>Perform clean utility sampling/monitoring on critical operating parameters for equipment and instrumentation to ensure standard operation (Weekends only)&nbsp;</li><li>Identify, report, and document deviations from established test methodologies, specifications, and alert limits. </li><li>Maintain up to date knowledge of cGMP, job related SOPs and complete all assigned training on time.&nbsp;</li><li>Coordinate sample receipt, logging, tracking, storage, distribution and archival.&nbsp;</li><li>Work closely with subject matter experts with regards to discrepancy reporting, investigations and CAPAs associated with the process.&nbsp;</li></ul>Qualifications &amp; Experience <ul><li>BS/BA in Biological, Chemical/Life Sciences, or its equivalent in experience.&nbsp;</li><li>Minimum 1 to 2 years of experience in a regulated microbiology laboratory preferred.&nbsp;</li><li>Excellent manual dexterity including proficiency in aseptic and pipetting techniques.&nbsp;</li><li>Experience executing Bioburden, autoclaves, micro-ID methods, and endotoxin testing.&nbsp;</li><li>Experience requiring one to work independently as well as part of a team, to complete assignments within defined time constraints.&nbsp;</li><li>Demonstrated ability to concurrently conduct multiple routine tasks, procedures, and operations effectively and consistently.&nbsp;</li><li>Attention to detail and demonstrated organizational skills. </li><li>Demonstrated ability to be resilient and adapt quickly in a fast-paced environment is essential. </li><li>Demonstrated ability to quickly learn and adapt to new information, technologies, and processes. </li><li>Demonstrated ability for efficient time management.</li><li>Knowledge of basic electronic systems including proficiency with Microsoft based platforms.</li></ul>This position is Sunday through Wednesday 1st shift position. 0700 – 1700.&nbsp;Contacts: Will work in teams and have continual interactions with team members as well as other sub-teams within and outside the Quality Control organization to exchange information regarding testing completion, in-process, and planned activities. Daily interaction with management and team leads. Routine contact with management for coaching and general performance management discussions. Occasional contact with other line management staff relating to specific projects may be expected.Working Conditions:QC Associates primarily work in GMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous material.Overtime work may be required on weekdays, weekends, holidays and during adverse weather conditions in support of manufacturing facility.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior QC Microbiology Associate, Lab Operations

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-usPosition OverviewSupervise an experienced team in the packaging and labelling of clinical supplies. Including oversight of the GMP, safety and procedural aspects of producing the supplies in a cGMP production area. Ideally, you will have pervious experience in pharmaceutical industry preferably, clinical trials packaging.Key Responsibilities <ul><li>Demonstrates a thorough working knowledge of the technical aspects of cGMP’s as they relate to clinical supply packaging and labeling.</li><li>Reviews the master production schedule and production orders, establishes production priorities and revises schedules according to production order specifications, establishing priorities for materials and staff.</li><li>Supervises staff in all aspects of packaging and labeling of clinical supplies. Maintain employee records (attendance, vacation etc.).</li><li>Assure all production orders are executed in accordance with cGMP's and SOP's. Utilizing SAP for error free technical documentation.</li><li>Establish and support a work environment of continuous improvements that supports the Company’s Quality Systems and the appropriate procedures for the area.</li><li>Utilizes technical writing skills to generate COSHH, Safety risk assessment, procedures and guidelines.</li><li>Interacts and liaises with team members from Packaging &amp; labelling, Quality, Logistics and Quality Control.</li><li>Oversees and or conducts training of new or existing employees and ensures their training is up to date and documented.</li><li>Ensures that health and safety guidelines are followed.</li><li>Leads root cause investigations for process deviations and assigns Corrective/Preventative Actions.</li></ul>Key Skills Required<ul><li>Prior Supervision of production staff or leadership role within a production operation with demonstrated ability in scheduling, organizing and team building</li><li>Working knowledge of cGMP’s and regulatory (i.e. MHRA, FDA, EU CTR, etc.) requirements and their application within a clinical packaging and labeling production environment.</li><li>Solid record of attention to detail and strict adherence to all procedures and regulations.</li><li>Good understanding of the pharmaceutical development process and associated scientific principles,</li><li>Demonstrated ability to communicate effectively with various support groups and able to lead in a team environment.</li><li>Effectively manage competing priorities, adaptable to change, demonstrated ability to accept additional responsibilities and mange tasks through teamwork.</li><li>Working knowledge of computers using MS Office, MS Outlook and business software systems commonly used in pharmaceutical industry (i.e. SAP, Veeva).</li><li>Demonstrates the ability to effectively schedule multiple jobs / orders.</li></ul>Education and Experience Required <ul><li>Bachelor of Science or a Mechanical Engineering Degree, required</li><li>Demonstrated experience in a pharmaceutical industry, required</li><li>Experience in Pharmaceutical manufacturing with a focus in the production of Clinical Trial Supplies, preferred</li><li>Extensive experience of progressive leadership or supervisory experience in the pharmaceutical industry, required.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.Bristol Myers Squibb is Disability Confident – EmployerA UK Government scheme

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