Description
This opening is with one of the most sought after Global pharma companies in the world, with this site being located here in the Bay Area. This position will be responsible for mainly for deviation resolution and Annual Product Reviews. At this time, only local candidates will be considered and interviews will begin immediately for qualified applicants. Primary functions include:- Prepare written QA evaluations of deviations investigations
- Resolve complex problems that require experience with quality systems and biologics manufacturing
- Create, implement and support deviation and CAPA tracking and trending systems
- Provide training and support for QA reviewers and Specialists
- Work closely with Quality Engineering to author and review APRs
- Present and discuss metrics during quality reviews
Mininmum Requirement
- B.S./B.A. in Biological Sciences or 6+ years required experience
- 3-4 years in Pharma manufacturing or QA on the Floor experience
- Experience with GMP/QSR/ISO as well as the following areas: purification, fermentation, Final Packaging and Quality Control
- Highly proficient in manufacturing investigations and root cause analysis
- Excellent communication skills
- Strong computer and presentation skills
Please send responses, inquiries and resumes to b.ross(@)realstaffing.com. Thank you for your interest.
To find out more about Real please visit www.realstaffing.com