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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

Bristol Myers Squibb is seeking a Manager, QC Sample Management for our Devens, MA Cell Therapy Facility. This role will manage the operations of the QC Sample Management Day Shift, responsible for the management of QC samples and materials in support of the QC laboratories. This includes, but is not limited to, mentoring, training, and managing the QC Sample Management team, maintaining and tracking testing samples, retains, scheduling lab operations, supporting lot release, creating and continuously improving processes, reviewing and approving documents, and overseeing sample tracking, delivery, and destruction.

This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required.

This role is stationed in Devens, MA and reports to the Associate Director of QC Systems and Support.

Key Responsibilities

• Provide supervision of QC Sample Management shift and oversee the daily Sample Management activities related to in-process, final release and stability testing of cell therapy drug product.

• Develop and manage a daily work plan for QC associates.

• Report out quality and operational metrics.

• Responsible for management of QC samples and materials including chain of custody, label, receipt, storage, transfer, and disposal according to GMP requirements and approved procedures. Facilitate cold chain transfers of samples, as required.

• Hire, mentor and develop the team members to support the business operations and employee career development.

• Oversee the training of the team members.

• Review and approve procedures for Sample Management activities.

• Collaborate with other departments to identify and implement process improvements.

• Own and evaluate relevant change controls, investigations, deviations, CAPAs.

• 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 assigned.

Qualifications & Experience

• Bachelor's degree required, preferably in Chemistry, Microbiology, or related science.

• 6+ years of relevant work experience, preferable in a regulated environment.

• 2+ years of management and people leader experience.

• An equivalent combination of education and experience may substitute.

• The incumbent will be working around biohazardous materials.

• The incumbent may be exposed to fluctuating and/or extreme temperatures on occasion.

• Experience with cold chain sample storage and transfer in a GMP regulated environment.

• Familiar with Excel, Visio, Power Point, and other software systems.

• Experience with laboratory LIMS and ERP systems (e.g., SAP) preferred.

• Ability to work in a highly regulated environment and follow regulatory requirements and GMPs.

• Ability to mentor associates, manage multiple assignment while meeting timelines in a GMP environment.

• Advanced ability to work in a collaborative team environment and train others.

• Advanced ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects.

• Excellent organizational and critical thinking skills.

• Advanced ability to communicate effectively with peers, department management and cross-functional peers.

#BMSCart, #LI-Onsite, #Veteran

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 adastaffingsupport@bms.com . 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.

Company: Bristol-Myers Squibb

Req Number: R1582426

Updated: 2024-06-26 01:20:56.355 UTC

Location: Devens-MA

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.