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Form of workJob Description
Our partner is a global healthcare leader in advanced technology throughout their businesses and products in diagnostics, medical devices, nutritional and medicines nationwide. They are seeking a QA Associate to join their team in Pomona, CA! This is a great opportunity to recieve industry best training, and work for a household name!
Responsibilities:
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
- The primary responsibility of the position is the review and approval of lot history records and control documentation to ensure GMP compliance of manufacturing operations and products. This includes the resolution of discrepancies, as well as review and approval of deviation and nonconformity reports.
- As a project team member; participate in team meetings, track metrics and report progress.
- Support Regulatory and client audits.
- Review document change requests.
Requirements:
- High School Diploma or Associates with Quality experience.
- Experience working in life sciences.
- Experience with GMP, and GLD.
Since 1995 Astrix has been delivering information technology consulting, regulatory advisory services and staffing solutions to the scientific community. We can assist in augmenting your internal resources to deliver optimum solutions on time and within budget. It is our goal to simply do it right. We work everyday to create value and build trust with our clients, employees, partners and vendors.
Astrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.
Astrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.
