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Job description
Quality Control SpecialistPerforms 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).Knowledge and skills: Required BS or Associate Degree - knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, 0-3 years of 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.)Decision Making: Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure.Supervision: Incumbents normally receive detailed instructions on routine work and detailed instructions on new assignments. No direct supervision.Work Environment: 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.
Worksite address
devens, MA, 01434, US
Who can apply
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