Analytical Development Documentation Reviewer - Contract - Bristol, PA
Ready to assist in bringing life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!
Primary Responsibilities:
You will be instrumental in ensuring data integrity, reviewing laboratory notebooks, and supporting GMP-related documentation processes. This role requires attention to detail and a collaborative approach to meet development goals.
Skills & Requirements:
The Analytical Development Scientist's responsibilities will be:
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at [email protected]
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