Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA

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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: Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition backed by a best-in-the-industry team and long-term commitment we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself accelerate your career and give new hope to patients theres no better place than here at BMS with our Cell Therapy team.

The Senior Specialist QC Materials Management Cell Therapy is responsible for the management of materials used in the analytical and microbiology QC laboratories in the Devens CTF ensuring the availability of all QC laboratory supplies. This includes but is not limited to managing the lifecycle activities of QC laboratory materials supporting onboarding of new materials through document creation and change control collaborating with QC network functions and site functions such as QC lab supply chain and other departments for the management of QC materials. The QC Material Management Senior Specialist will also serve as the QC Material Management SME supporting training document revisions projects CAPA and related tasks and/or continuous improvement efforts.

Shifts Available:

TBD

Responsibilities:

• Serve as the site representative for QC material management program and manage the lifecycle activities of QC laboratory materials.
• Support onboarding of new materials through document creation and change control.
• Collaborate with QC network functions and site functions such as QC lab supply chain and other departments for the management of QC materials.
• Implement and maintain the QC material inventory management system (e.g. Kanban).
• Train others on material management process and procedures as applicable.
• Perform document revision project CAPA and related tasks and/or continuous improvement efforts.
• Create revise and review technical documents such as SOPs and working instructions for sample management.
• Implement 5S and FIFO principles as appropriate.
• Apply critical thinking skills when working on new procedures or process improvements.
• Communicate effectively with management regarding task completion roadblocks and needs.
• Perform other tasks as required to support the QC laboratories.

Knowledge Skills Abilities:

• Ability to accurately and completely understand follow interpret and apply Global Regulatory and cGMP requirements.
• High problem-solving ability/mentality technically adept and logical.
• Ability to communicate effectively with peers department management and cross-functional peers about task status roadblocks and needs.
• Ability to work in a fast-paced team environment meet deadlines and prioritize work.
• Excellent organizational and critical thinking skills.

Minimum Requirements:

• Bachelors degree preferably in Chemistry Microbiology or related science. Advanced degree preferred.
• 4 years of relevant work experience preferably in a regulated environment. An equivalent combination of education and experience may substitute.
• Experience with material management and supply chain processes preferred.
• Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS preferred.
• Experience in writing and revising GMP procedures and working instructions.

Working Conditions:

• The incumbent will be working around biohazardous materials and may be exposed to fluctuating and/or extreme temperatures on occasion.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

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.

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The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job such as required skills where the job is performed the employees work schedule job-related knowledge and experience. Final individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical pharmacy dental and vision care. Wellbeing support such as 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. Work-life programs include paid national holidays and optional holidays Global Shutdown Days between Christmas and New Years holiday up to 120 hours of paid vacation up to two (2) paid days to volunteer sick time off and summer hours flexibility. 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.

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