Quality Control Technician

$32.23/hr

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


Duties and Responsibilities:
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 and responsibilities of the specific QC sub-team. Assignments are made in the LIMS by the hiring manager, following the applicable curricula map(s).

Knowledge and Skills:
Required Associate Degree but prefer BS knowledge of science generally attained through studies resulting in a BS in the physical or life sciences or a related discipline, with 0-3 years of experience.
Familiarity with basic laboratory techniques such as pH, appearance, volumetric measurement, pipetting, analytical weighing, and basic laboratory safety practices is preferred.
Attention to detail and solid organizational skills are essential.
Demonstrated manual dexterity is required.
Knowledge of basic electronic systems (email, MS Office, etc.) is expected.

Decision Making:
Associates should be proactive in observing their work area and tools, and are expected to identify and report any discrepancies from standard practice or procedure.

Supervision:
Incumbents typically receive detailed instructions on routine work and on new assignments.
This role does not include direct supervision responsibilities.

Work Environment:
There will be daily contact with supervisory staff for work assignments, as well as routine discussions for coaching and general performance management.
Occasional interactions with other line management staff related to specific projects may also be anticipated.