Description
This large pharmaceutical company has an enormous presence here in the Bay Area and a solid number of pipelined and commercial products. They are looking to bring on multiple validation personnel to bolster the team as they continue to grow. We need candidates who are enthusiastic and excited about the opportunity to join a stable and highly regarded company.Job description as follows;
- Collaborates with internal and external technical and management personnel to establish project priorities, goals, structure, and optimization of validation approaches.
- Develops, executes, and analyzes validation projects to demonstrate process consistency, facility, equipment and cGMP compliance to FDA and EMA regulations and ICH guidelines.
- Evaluates internal equipment and systems, develops and applies test protocols
- Interfaces between various internal and external functional areas to assure successful integration and completion of validation activities in overall project schedules.
- Applies quality standards, policies, procedures, and knowledge of current industry/regulatory standards for validation implementation, execution and completion
- Reviews change controls for new and upgraded processes, analytical methods, computer systems, equipment, and facilities
The candidate would ideally have;
- 3+ years of related pharmaceutical industry experience
- Excellent written and oral communication skills
- Demonstrated knowledge of fundamental cGMP concepts
- Proven ability to handle multiple projects and meet deadlines
- Precise attentio to detail
If you feel that you meet these requirements and are interested in finding out more or interviewing, please contact b.ross(@)realstaffing.com with resume and/or contact information.
Thank you so much for your time and interest!!
To find out more about Real please visit www.realstaffing.com