Description:

Lead and support Commissioning & Qualification (C&Q/CQV) activities for GMP facilities and systems.
Develop, review, and execute C&Q deliverables including protocols and qualification reports.

Requirements:

Bachelor’s degree in Engineering, Life Sciences, or related field.
5+ years of experience in C&Q/CQV within regulated environments.
Strong knowledge of C&Q methodologies and GMP regulations.
Kneat Power User Level 1 certification preferred.
Experience with project/test-management platforms and electronic document management systems.
Strong communication and organizational skills.
Ability to manage multiple priorities in a global project environment.

Benefits