Job description
Quality Control Associate
Job Description:
Job Responsibilities:
Minimum Qualifications:
Preferred Qualifications:
About The Company:
#ZR2
- Contract Duration 7 Months
- Pay range $27/hr - $36/hr
Job Description:
- Our client is seeking a contractor for Quality Control Associate I position based at their Norwood, MA site.
- The individual in this role will perform cGMP QC testing for QC Chemistry.
- The position will be 3rd shift to cover Wed-Sat rotation and may require off-shift hours.
Job Responsibilities:
- Performs routine analytical chemistry testing including HPLC, UPLC, UV, Particle Analysis, and Dynamic Light Scattering.
- Performs data entry and supports data review as assigned.
- Quality Control Associate performs general laboratory support activities including reagent preparation, equipment maintenance, lab housekeeping, etc.
- Write/revise SOPs, technical protocols, and reports.
- Works with and within the LIMS system to record data and associated testing details.
- Perform HPLC (AEX) and NaOH plate reader-based assays in support of manufacturing process stat testing as needed.
- Supports sample management activities including sample retrieval/ receipt, sample logging, aliquoting, and distribution.
- Orders, Manages, and monitors stocking of QC lab supplies
- Complete and maintain cGMP documentation for work performed.
- Establish and maintain a safe laboratory working environment.
- Support testing for raw materials, intermediates, drug substances,s and drug products, including the generation of testing data to support clinical studies.
- Assist in the development, implementation, and maintenance of general laboratory operational systems in accordance with cGMP requirements.
- May assist with equipment qualification/validation activities, including maintenance.
- May troubleshoot issues related to equipment, laboratory procedures, and assay performance.
Minimum Qualifications:
- BS in a relevant scientific discipline
- At least 1 year of relevant experience in a cGMP organization with a focus on GMP testing
Preferred Qualifications:
- A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
About The Company:
- Our client operates as a developer of messenger RNA therapeutics. The company develops and discovers drugs that produce proteins or antibodies inside patient cells. Its pipeline includes various drug modalities such as prophylactic vaccines, therapeutic vaccines, intratumoral immuno-oncology, localized therapeutics, and liver intracellular. Through its mRNA therapeutics platform, they develop and produce human proteins, antibodies, and Client proteins, which help in preventing, treating, and curing diseases. It also develops therapeutics in the areas of infectious disease, rare liver disease, immuno-oncology, and cardiovascular disease.
- mRNA is now a turning point in the history of science, medicine, technology, and even humankind itself. With this breakthrough discovery, many of the world’s biggest and most challenging medical problems are no longer a question of “how?” but merely a question of “when?”
- Come with us as we pursue the uncharted reaches of possibility and make your mark on the future of medicine.
#ZR2
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