A multinational pharmaceutical contract manufacturer recently required the assistance of a senior pharmaceutical QA resource to assist with managing Quality and GMP issues at their manufacturing site.
SeerPharma was able to secure a contract resource with over 25 years of experience in the industry to work on site and assist their team with managing issues such as corrective and preventive actions (CAPA), reporting and GMP training. Our resource was deployed for 3 months and was well received by the client’s senior management and staff.
A number of our clients have turned to SeerPharma of late for a variety of contract resources. From junior level technical writing and validation roles to Director level positions. Having been in the industry for over 25 years, and with a wealth of personal connections and networks, we have extensive reach to be able to locate and find talented individuals.
Contact us should you need a contract resource to assist with your Quality Assurance affairs.
This post comes from our October 2016 Journal. You may also be interested in these posts:
- Effective CAPA in a GMP Environment
- GMP - What you need to know (Training)
- The Importance of Product Quality Reviews (PQRs)
