Senior Specialist, QC Materials Management, Cell Therapy
Senior Specialist, QC Materials Management, Cell Therapy
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Job Description
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. 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: 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 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.
The QC Materials Management Senior Specialist role is stationed in Devens MA and reports to the Associate Director QC Systems and Support.
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 and Skills:
- 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.
Basic 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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If you come across a role that intrigues you but doesnt 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.
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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 a supportive culture promoting global participation 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 an 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 . Visit 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.
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Required Experience:
Senior IC
Employment Type
Full-Time
