Job Information
Bristol Myers Squibb Specialist, QC Sample Management, Cell Therapy in Warren, New Jersey
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 .
Title: Specialist, QC Sample Management, Cell Therapy
Location: Warren, NJ
At 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, there's no better place than here at BMS with our Cell Therapy team.
The Specialist, QC Sample Management, Cell Therapy is responsible for performing routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition. Owns the periodic sample and data inventory maintenance activities. May support testing scheduling/planning for QC testing.
This po sition will support the weekend shift as well as intermediate shift over the week., Wednesday to Sunday 12 - 8:30PM.
Key Responsibilities:
Perform routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition.
Owns the periodic sample and data inventory maintenance activities.
Performs data compilation, lot and sample Chain of Custody (COC) data review, and review of GMP documentation.
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
May support testing scheduling/planning for routine QC testing such as in process, release, stability testing and non-routine sample testing.
Provide support and training to the organization with respect to scheduling tools.
Train analysts on general job duties.
Compiles lot files for QC disposition review.
Generate SOTR and manual CoA.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform other tasks as assigned.
Qualifications & Experience:
Bachelor's degree or equivalent required, preferably in science.
4+ years of relevant LIMS or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in LIMS and knowledge of Chain of Identity and Chain of Custody.
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated knowledge of LIMS, ELN and laboratory data analysis systems.
Problem-solving ability/mentality, technically adept and logical
Ability to communicate effectively with peers, department management and cross-functional peers.
Demonstrated technical writing skills
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
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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: R1583192
Updated: 2024-07-07 02:02:49.870 UTC
Location: Warren-NJ
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.