Associate Quality Control
3 Key Consulting
Associate Quality Control
3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Under general supervision, this position will perform routine procedures and testing in support of the High Throughput lab (HTL) group. This position will be responsible for one or more of the following activities:
- Performing routine laboratory procedures.
- Routine analytical testing.
- Documenting, computing, compiling, interpreting and entering data.
- Maintaining and operating specialized equipment.
- Initiating and/or implementing changes in controlled documents.
Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Supplement additional workload on team.
Top must-have skill sets:
- Prior lab experience.
- cGMP experience.
- Chemistry/Biochemistry background.
Day to day responsibilities:
- Routine analytical testing - documenting, computing, compiling, interpreting and entering data.
- Maintaining and operating specialized equipment.
- Initiating and/or implementing changes in controlled documents.
- Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
- General lab housekeeping.
Unique experience and opportunity.
Red flags:
Lack of lab experience.
Interview process: Phone screening followed by in-person interview.
Vacancy posted 4 days ago
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