Job Overview:
A senior validation professional is required to lead CQV work on various projects, including bulk processing and facilities upgrades.
Key Responsibilities:
* Develop and execute commissioning, qualification, and validation protocols for equipment and processes.
* Prepare detailed documentation, including URS, FRS, IOQ, and PQ protocols.
* Coordinate risk assessments and impact assessments for new systems.
* Collaborate with cross-functional teams for timely project delivery.
* Troubleshoot and resolve issues during the CQV process.
* Maintain compliance with cGMP, FDA, and relevant regulations.
* Provide training and guidance to operational staff on validated systems.
Requirements:
* Bachelor's Degree in Engineering/Science/Technical.
* Minimum 5+ years pharmaceutical industry experience.
* Experience in process, fill/pack and utility systems.
We offer a competitive package and opportunities for career growth.