Vacancy expired!
Piper Companies is currently seeking a QA Associate for an innovative Biotechnology company focused in research in the Rockville, MD area.
Responsibilities for the QA Associate include:- Manage executed cGLP documentation and other documents relating to cGLP activities
- manage the audit process
- Initiate new SOPs and/or revise existing SOPs as needed
- The managing of Deviations, Change Controls, CAPAs and Out of Specification events
- Review and approval of CGLP logbooks
- Review, approval and release of raw materials for use in CGLP manufacturing and testing
- Perform room clearances
- Assist in FDA inspections regarding regulated activities
- Occasional weekend and evening work will be required
- Present cGLP training programs
- College degree in chemistry, biology or related field of study
- 2+ years of GLP experience
- Salary Range: based on experience
- Comprehensive Benefits: Healthcare, Dental, Vision
Vacancy expired!