Specialist, QC Analytical in Devens, MA
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Job Location:
Devens, MA - USA
Monthly Salary:
$ 40 - 48
Posted on:
4 days ago
Vacancies:
1 Vacancy
Job Summary
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 Specialist QC Analytical Cell Therapy is responsible for supporting QC testing for in-process final product and stability samples including data review/verification. May assist with method transfer documentation deviations investigations and continuous improvement efforts.
Shifts Available:
Wednesday Saturday 2pm 12am (including holidays)
Responsibilities:
- Perform routine testing of in-process final product and stability samples.
- Perform testing for method transfer/validation/verification.
- Perform data verification data review and review of GMP documentation for general methods.
- May perform document revision project CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
- Train analysts on general job duties.
- Perform other tasks as assigned.
Knowledge and Skills:
- Ability to accurately and completely understand follow interpret and apply Global Regulatory and cGMP requirements.
- Knowledge of LIMS ELN and laboratory data analysis systems preferred.
- Problem-solving ability/mentality technically adept and logical.
- Ability to communicate effectively with peers department management and cross-functional peers.
- Experience with writing technical documents preferred.
- Ability to work in a fast-paced team environment meet deadlines and prioritize work.
Basic Requirements:
- Bachelors degree or equivalent required preferably in science.
- 2 years of relevant analytical testing or QC experience or equivalent combination of education and experience preferably in a regulated environment.
- Demonstrated experience in cell and molecular biology techniques (e.g. cell-based assays flow cytometry qPCR ELISA and aseptic technique).
BMSCART
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GPS2025
Key Skills
- Academics
- Ale
- Asset Management
- Legal Operations
- Art And Craft
- Database Administration
About Company
Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more
