A company that manufactures, fills, and packages a wide-range of consumer, over the counter, and personal care products is seeking a Quality Assurance Associate.
Description:
Ensure compliance to cGMP standards in the Manufacturing and Packaging areas.
All production control records have been compiled and are complete and accurate.
All Laboratory Services release testing showed satisfactory conformance to bulk and finished product specifications.
Execute or coordinate the resolution to excursions identified during the batch review process.
Issue and perform review of logbooks and notebooks.
Review and approve shipper labels for use.
Review lot codes during packaging record issuance.
Compile, organize, and review documentation from customers, Manufacturing, Packaging, and Laboratories.
Adherence to customer release requirements.
Update paper and electronic records.
File and archive documentation.
Skills & Qualifications:
1+ years of professional experience in a QA/QC position within a GMP environment preferred.
Bachelor’s degree in a science related field preferred.
LIMS or other laboratory database experience preferred.
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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