EGLS has an excellent opportunity for a Senior CSV Consultant with a client in the Pharmaceutical Industry. This position will act as the CSV Lead for a very important systems merger project.
Our client is looking for:
- 8+ years of experience in the Pharmaceutical or Bio-Pharmaceutical Industries.
- Thorough knowledge of validation life cycle, validation protocols (IQ/OQ/PQ) generation and execution of manufacturing and laboratory equipment.
- Fundamental understanding of validated computer systems and change management in the commercial pharmaceutical/biotech industry, including training others.
- GMP compliance knowledge including knowledge of 21 CFR Parts 210, 211, 11, EU Annex 11. among others.
- Demonstrated experience in management of complex tasks and projects.
- Proficient at establishing clear and understandable directions and goals. Provides and implements suggested resolution to roadblocks.
- Able to prioritize own work and aid in setting group priorities
- Strong organizational skills.
