QA In-Process Quality Engineer
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Accentuate Staffing is partnering with a global pharmaceutical company who is hiring for QA In-Process Quality Engineers. This is a direct hire opportunity, offering competitive pay and benefits, working onsite. The ideal candidate will have a strong background with quality assurance in GMP regulated, pharmaceutical environments.
The shift is a 2/2/3 schedule (working every other weekend). 12 hours shifts. Openings on 1st and 3rd shift. 1st shift: 5AM to 5PM. 3rd shift: 5PM to 5AM.
Responsibilities:
1. Ensures continuous compliance to the facilities SOPs and cGMPs for all production and packaging.
2. Quality Assurance reviews and approvals for batch records and all associated documentation for production.
3. Authoring and performing CAPAs, investigations, deviations, root cause analysis and OOS.
4. Multi-task, balancing multiple priorities and tasks in a fast paced environment.
Requirements:
1. Associates or Bachelors degree in a Scientific field.
2. No less than two years of experience in a pharmaceutical quality assurance or manufacturing environment.
3. Clearly demonstrated work history of good documentation practices (GDP).
4. Must have experience with CAPAs, deviations and root cause analysis.
