Lenox Executive Search is seeking a Quality Control Analyst for a
CONTRACT
position with one of our global pharmaceutical clients. This a
ONE-YEAR CONTRACT
role fully onsite in Lexington, MA.
- Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations.
- Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods.
- The assays range from pH, enzyme concentration to more complex assays such as SDS silver Gels, PCR, DNA and enzyme activity.
- This position is expected to maintain operational and GMP readiness of the QC areas.
- In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems.
Specific QC Focus Area:
Biochemistry Focus:
A280, SOLO
A280, Compendial methods (pH. Moisture, OSMO, Appearance, Subvisible particles), Enzyme Activity assays,
DNA, PCR, Free Thiol Responsibilities:
- 80% Testing execution
- 10% QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab housekeeping, support for other QC groups if needed.
- 10% Compliance and quality systems (SOP revisions, input to quality system
Education and Experience Requirements:
- Bachelor's degree and minimum of 0-2 years related experience
Desired:
GMP knowledge, work experience
- Limited use and/or application of basic principles, theories and concepts.
- Limited knowledge of industry practices and standards.
Position requires critical thinking. MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understanding readily obtained. Builds stable working relationships internally.
Pay:
$38.00 per hour
Work Location:
In person