Waltham, MA | Contract to Hire
- Organize scientific study, review, interpret data and draw reasonable conclusions.
- Write appropriate method transfer/validation protocols and corresponding reports.
- Provide expert ownership for the completion of planned analytical activities in accordance to agreed scope and timing under the oversight of the AD representative.
- Must have Small Molecule Experience
- Support technical guidance for active pharmaceutical ingredient and drug product (DP) analytical method validation and transfer activities.
- Provide technical collaboration and support integrated planning with the clients internal CMC teams and associated CMO/CRO organizations.