Job Requirements:
- Has worked within QC Method Validation Transfer (experience with method validation and transfer) MUST
- Leading validation of release test methods for monoclonal antibody product in late-phase development.
- Expertise with protein purity methods (SEC, CE-SDS and cIEF, for example) and prior experience working in GMP laboratory is required.
- Experience with CMO’s/ contract test labs required (inclusive of strong communication and trouble-shooting analytical methods).
- Prefer MS or PhD in chemistry/ biochemistry field
- Prefer someone who is not more than 10 years out of the lab. (please ask them this question and have the exact number)
- Be able to work independently
- Past Pfizer/biogen experience is a plus
Remote: QC Method Validation Consultant (237158)
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