Job Description

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

PURPOSE AND SCOPE OF POSITION:

The QC Scientist, Sample Management is responsible for the management of all QC samples and

materials in support of the analytical and microbiology laboratories at the CAR T manufacturing

facility in Summit, NJ. This includes, but is not limited to, inventory management, retain

management, sample tracking, and sample delivery.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

* Proficient in the use of LIMS and sample tracking software.
* Working knowledge of lean laboratory principles.
* Proficient with enterprise application software.
* Experience with cold chain sample storage and transfer.
* Advanced ability to work in a collaborative team environment.
* Advanced ability to accurately and completely understand, follow, interpret, and apply global regulatory and GMP requirements.
* Ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.
* Ability to set priorities of the sample management group and manage timelines.

Education and Experience:

* Bachelors degree required, preferably in Chemistry, Microbiology, or related science.
* Advanced degree preferred.
* 5 - 8 years of relevant work experience, preferably in a regulated environment.
* An equivalent combination of education and experience may substitute.

DUTIES AND RESPONSIBILITIES:

Manages test samples and retains including:

* Managing test samples throughout the sample lifecycle- receipt, storage, distribution, transfer, and disposal.
* Managing long-term storage of retains and reference samples.
* Maintaining sample tracking and chain of custody records in accordance with GMP requirements and written procedures.
* Ensuring that obsolete or expired samples and materials are destroyed and disposed of according to written procedures.
* Performing sample queries and periodic storage reports, as required.
* Assisting management with investigations and deviations related to sample management.
* Collaborating with other departments to identify and implement process efficiencies.
* Training laboratory and production personnel on the sample management process.

Manages laboratory inventory including:

* Managing the inventory of laboratory supplies including reagents, media, consumables, etc.
* Managing the reference standard inventory and distributing reference standards to functional groups, as necessary.
* Ensuring that materials are appropriately labelled and tracked according to GMP regulatory requirements, and written procedures.
* Assisting management with investigations and deviations related to laboratory inventory.
* Implementing 5S and FIFO principles, as appropriate.

Provides QC materials support including:

* Maintaining metrics for the sample management group.
* Facilitating cold chain transfers of samples, as required.
* Collaborating with supply chain, warehouse, and lab services to ensure all QC laboratory supplies are adequately stocked.
* Performs other tasks as assigned.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or 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.