Job Summary:
We are seeking a highly skilled CQV Specialist to join our team in the biopharmaceutical industry.
This is an exciting opportunity for a motivated professional to leverage their technical expertise and passion for quality assurance to drive success in a dynamic environment.
About the Role:
The CQV Engineer will be responsible for commissioning and qualifying new aseptic manufacturing equipment, writing and executing qualification documentation, and providing technical assistance during investigations or process/equipment troubleshooting.
Key Responsibilities include ensuring on-time execution of schedules, managing periodic review plans, collaborating with various departments/teams, and ensuring validation activities meet company and regulatory requirements.
The ideal candidate will have previous experience in aseptic equipment/qualification/aseptic processing, advanced knowledge of FAT, SAT, IOQ risk-based verification, and experience with Kneat/online validation package.
Requirements:
Motivated CQV Specialist seeking a challenging role in the biopharmaceutical industry with a strong desire to grow professionally in a dynamic and innovative work environment.
Benefits:
This role offers competitive compensation packages and opportunities for professional growth in a dynamic and innovative work environment.