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Quality Assurance Supervisor, Pharmaceuticals

Location : Morris Plains NJ US 07950
Job Type : Temp/Contract to Direct
Reference Code : 20237-JF1
Compensation : open - 50-55/h
Start Date : 06/26/2020
Hours : Full Time
Required Years of Experience : 10
Required Education : BS Life Sciences
Travel : No
Relocation : No
Job Industry : Pharmaceutical

Job Description :


  • Contract to direct position for a Quality Assurance Supervisor for pharmaceutical manufacturing.

  • Manage and perform activities related to QA oversight of manufacturing, packaging/labeling, inspection, QC laboratory, and plant maintenance / engineering.

  • Ensure that all products manufactured at the site and contract manufacturing organizations meet all established specifications, cGMPs, and all associated regulatory requirements.

  • Responsible for the review and approval of executed batch records, and final disposition of all commercial products.

  • Maintain acceptable GMP regulatory compliance and quality performance.

  • Prevent and mitigate quality risks which can jeopardize company's interests (patient safety, supply continuity, reputation).

  • Responsible for the review and approval of executed batch records: media fills, compounding, filling, capping, terminal sterilization, visual inspection, labeling and packaging.

  • Release of final packaged product for shipping to offsite warehouse.

  • Meet department metric for schedule adherence.

  • Oversee team of QA employees responsible for the oversight of manufacturing, packaging, labeling, inspection, QC laboratory, plant maintenance and engineering.


Required Qualifications :


  • BS in Life Sciences or Pharmacy.

  • Minimum 10 years of total business experience in the pharmaceutical or biotechnology industry.

  • Minimum 7 years of progressive experience in QA related functions.

  • Minimum 5 years supervisory experience is required.

  • Experience with Quality Control, Supplier Quality, GMP Manufacturing or Technical Services is highly preferred.

  • Experience with Aseptic sterile pharmaceutical manufacturing and facilities is highly preferred.

  • Experience with Trackwise software required.



Contact: John Forsatz


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