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SENIOR ASSOCIATE, QC OPERATIONS

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb.
Around the world, we are passionate about making an impact on the lives of patients with serious disease.
Empowered to apply our individual talents and ideas so that we can learn and grow together.
And driven to make a difference, from innovative research to hands-on community support.
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 the resources to pursue their goals, both at work and in their personal lives.
Bristol-Myers Squibb has announced plans for an expansion of its large-scale biologics manufacturing facility in Devens, Massachusetts.
The expansion will create a mammalian cell biologics center of excellence through the introduction of biologics development and clinical trial manufacturing capabilities to the site.
Both represent new capabilities for Devens, a site that in its early years has focused solely on large-scale, bulk biologics manufacturing.
Our Devens site has an opening for a Senior Associate, QC Operations to work 2 PM- Midnight Sunday- Wednesday.
Responsibilities:
Perform routine Bioburden, Endotoxin, and environmental monitoring testing in accordance with SOPs, safety, and cGMP guidelines to support the release and stability of finished products, raw materials, in-process materials, and various components.
Perform clean utility sampling Monitor critical operating parameters for equipment and instrumentation to ensure standard operation.
Recognize, report, and document deviations from test methodologies, specifications, and alert limits Maintain up to date knowledge of cGMP, job related SOPs and complete all assigned training on time.
Coordinate sample receipt, logging, tracking, storage, distribution and archival.
Qualifications BS/BA in biological sciences, or its equivalent.
A minimum of 2 years experience in a regulated microbiology laboratory.
Excellent manual dexterity including proficiency in aseptic techniques.
Familiarity with the use of air sampling equipment, autoclaves, micro ID methods, and endotoxin testing.
Experience requiring one to work independently as well as part of a team, to complete assignments within defined time constraints.
Demonstrated ability to concurrently conduct multiple routine tasks, procedures, and operations effectively and consistently.
Bristol-Myers Squibb is an equal opportunity employer - Vet/Disability - 1501672

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