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Quality Control Associate

Job Title: QC Associate

Location: Devens, MA

Duration: 12 Months

Comments: 100% onsite- Mon-Fri (normal business hours)

Must haves:

  • Knowledge of science generally attained through studies resulting in a BS degree, preferably in Chemistry, Molecular Biology, or related discipline. degree preferred
  • Experience with cGLP or cGMP.
  • High attention to detail with strong general laboratory and good organizational skills.
  • Demonstrated ability to work independently as well as part of a team, to complete assignments within defined time constraints.

Job Description:

Performs routine testing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment.

Executes routine procedures based on methodologies/responsibilities of the specific QC sub-team. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).

Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within QC, in order to exchange information regarding testing completed, in process and planned.

Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions.

Occasional contact with other line management staff relating to specific project responsibilities may be expected.

Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.

Overtime work may be required on weekdays, weekends, holidays, and during adverse weather conditions in support of manufacturing facility.

Flexibility to work irregular hours and short notice overtime.

KNOWLEDGE/SKILLS REQUIRED/EDUCATION

  • Knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, or the equivalent in related experience.
  • Knowledge of basic laboratory techniques such as pH, volumetric measurement, pipetting, analytical weighing and basic laboratory safety practices preferred.
  • Attention to detail and demonstrated organizational skills.
  • Demonstrated manual dexterity.
  • Knowledge of basic electronic systems (email, MS Office, etc.)

Job Types: Full-time, Contract

Salary: $40.00 - $45.70 per hour

Schedule:

  • 8 hour shift
  • Day shift

COVID-19 considerations:
Candidate has to be fully vaccinated.

Work Location: One location

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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.

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DATE POSTED
June 10, 2023

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