Description
We are actively searching for strong candidates to be considered for this QA role with a large, global Pharmaceutical company in the Bay Area, CA. This will be a QA oversight role of manufacturing and will work on compliance and quality issues within the Process Unit. Main responsibilities will involve deviation management, auditing and operational oversight. This is a great opportunity for job stability as you would be joining a well established company. Schedule flexibility would be a plus and an expert knowledge of cGMPs is a must.Description:
- Responsible for ensuring Compliance with federal regulations and company SOPs
- Oversight of Raw Material realease and Commercial Product
- Coordinate investigations and CAPAs with all operating units
- Quality and Compliance oversight to all operations on shop floor
- Deviation management, including decision making in regards to critical/major deviations
- Internal audit coordination
- Participate in proces improvements, record and analyze metrics
- Compile data and author risk assesment reports
Requirements:
- 10+ years of related Pharmaceutical experience
- Batch disposition and deviation management experience
- Expert, up to date knowledge of cGMPs
- Excellent oral and written communication skills
- Proven leadership ability and willing to work under minimal direction
- Stron computer skills. SAP and Trackwise exp. is a plus
If you are interested in this exciting opportunity, please send your information to b.ross(@)realstaffing.com for more information or to apply. Local candidates will be preferred. Thank you for your interest!
To find out more about Real please visit www.realstaffing.com