Job Title: QC Associate
Location: Devens, MA
Duration: 12 Months
Comments: 100% onsite- Mon-Fri (normal business hours)
Must haves:
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
Job Types: Full-time, Contract
Salary: $40.00 - $45.70 per hour
Schedule:
COVID-19 considerations:
Candidate has to be fully vaccinated.
Work Location: One location
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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