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