Technician 2, QC Sample Management, A1 shift, Cell Therapy

About the role

Bristol Myers Squibb is seeking an Associate for QC Sample Management at the Cell Therapy Facility (CTF) in Devens, MA. This role is responsible for the movement and control of QC samples and materials, including in-process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories.

Responsibilities

• Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal.
• Facilitate cold chain transfers of samples.
• Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling, and chain of custody records in accordance with regulatory requirements and written procedures.
• Maintain inventory and distribution of QC samples and materials to functional groups as scheduled or requested.
• Maintain 5S and FIFO principles, as appropriate.
• Support performance metrics for the sample management group.
• Support investigations through data gathering or interview process.
• Collaborate with other departments to identify and implement process efficiencies.
• Communicate effectively with management regarding task completion, roadblocks, and needs.

Qualifications and Education Requirements

• Experience with cold chain sample storage and transfer in a GMP regulated environment.
• Knowledge of basic electronic systems (email, MS Office, etc.).
• Experience with LIMS and ELN computer applications preferred.
• Able to perform light to moderate lifting and carrying objects up to 20 lbs.
• Knowledge of regulatory standards as they apply to GMP laboratories is preferred.
• Attention to detail and demonstrated organizational skills.
• Ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.
• Ability to work in a high-paced team environment, meet deadlines, and prioritize work.
• Ability to communicate effectively with peers, department management, and cross-functional peers.
• Bachelor’s degree, preferably in Chemistry, Microbiology or related science, with 0-2+ years of relevant work experience, preferable in a regulated environment; or Associate degree with 2+ years of relevant experience.

Other Equivalent Combination of Education and Experience May Substitute

The incumbent will be working around biohazardous materials and may be exposed to fluctuating and/or extreme temperatures on occasion.

Job Location and Schedule

This role is stationed in Devens, MA and reports to Shift Manager of QC Sample Management. 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.

Compensation

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.

Benefits

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.