Senior Specialist, QC Analytical, Cell Therapy

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. 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.

Senior Specialist, QC Analytical, Cell Therapy

The shift for this position is B2 (2pm-12am, Wednesday-Saturday).

Position Summary

Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.

Duties/Responsibilities

·         Perform method transfer/validation and routine testing of in-process, final product, and stability samples.

·         Anticipate and perform routine troubleshooting and problem solving with minimal guidance.

·         Perform data verification, data review and review of GMP documentation for general and complex methods.

·         Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.

·         Train and mentor others on QC test methods, processes and procedures.

·         Perform other tasks as assigned.

Reporting Relationship

·       This position will report to QC management.

Qualifications

Specific Knowledge, Skills, Abilities:

·         Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.

·         Demonstrated technical writing skills.

·         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.

·         Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.

Education/Experience/ Licenses/Certifications:

·       Bachelor's degree or equivalent required, preferably in science.

·       4+ 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).

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.

Devens - MA - US: $43.84 - $53.12per hour

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 employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be d