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We have an opportunity for an experienced QC Support Specialist to join a global pharmaceutical company that focuses on vaccines. This is an excellent opportunity contributing to helping protect the lives of millions of people across the world.
The main purpose of the QC Support Specialist is to provide support to the QC Compliance and Improvement Manager across the site's QC activities.
Key Responsibilities:
1. Work closely with the labs to lead Deviations, CAPAs, and Change Controls through to on-time completion.
2. Participate in lab improvement projects, innovation, and improvements regarding equipment and new technologies.
3. Ensure appropriate standards of cGMP, Housekeeping, Health, Safety, and Environment are applied in all activities, in accordance with current regulations and procedures.
4. Support QC labs with respect to sample delivery.
5. Keep oversight of and facilitate on-time completion of DRs, CAPAs, Change Controls, and SOP Updates.
6. Monthly and annual report writing for EM, Bioburdens, and Endotoxin results, including annual product review.
Qualifications/Experience:
1. GMP experience within the Pharmaceutical industry.
2. Understanding of QC within a Lab.
3. Deviation investigation experience (necessity).
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