Job Title: Validation Specialist - GMP Environment
We are seeking a skilled Validation Specialist to join our team in a dynamic, GMP-regulated environment. As a key member of our validation team, you will play a crucial role in ensuring our validation systems are compliant, robust, and well-documented.
About the Role
The successful candidate will be responsible for developing, executing, and documenting validation protocols and reports across process, cleaning, equipment, analytical instruments, and utilities. This includes ensuring all validation activities align with GMP requirements and regulatory guidelines.
* Developing and executing validation protocols and reports
* Maintaining accurate and complete validation documentation
* Supporting technology transfers and new product introductions
* Collaborating closely with manufacturing quality engineering teams to coordinate validation efforts
The ideal candidate will have excellent documentation skills as well as strong organizational skills. You will also possess exceptional communication skills to effectively collaborate with cross-functional teams.
Skills & Qualifications
The successful candidate should have:
rules engineering or pharmaceutical science degree (or related field). 24 years of experience in validating within a gmp regulated environment.
good knowledge of gmp regulations.
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