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 a Sr. Validation Engineer 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