What are the responsibilities and job description for the Manufacturing Quality Associate position at Quality Compliance Partners, Inc.?
Manufacturing Quality Associate
Contract opportunity to join our team of quality professionals to support pharmaceutical/biotech manufacturing quality in an FDA-regulated environment.
Responsibilities:
Will be responsible for assisting with various aspects of quality assurance in an FDA-regulated manufacturing environment. Responsibilities will be dependent upon experience, and may include, but are not limited to, raw material release, line clearances, visual inspections, document control, preparation of manufacturing labels, review of manufacturing batch records and/or review of QC data.
Skills:
- Must have quality assurance experience in an FDA GMP manufacturing environment
- Understanding of manufacturing processes
- Strong Attention to detail
- Strong verbal and written communication skills
- Excellent interpersonal skills
- Minimum of 2-3 years of relevant experience.
- Preferably educational background in the sciences (Engineering, Biology, Chemistry).
Local Candidates only please as this position is on-site
No 3rd parties
Job Types: Full-time, Contract
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person