Quality Consultant - Part Time
Collaborations Pharmaceuticals is looking for a Quality Consultant to support upcoming GMP production for a Phase 1 enzyme replacement program. We need support with drug substance and drug production vendor oversight. In addition, we need support with the company’s Quality systems including training program oversight from time to time.
This is a part-time consulting position. We are flexible for location whether local to our homebase in RTP or remote. There will be some travel required for multiple quality audits.
The role may also include participation on grant and contract proposals for future projects.
Desired qualifications are prior experience with leading the Quality efforts for small batch Phase 1 rare disease parenterals. Experience helping and advising small companies on the Quality side with phase appropriate development in size and complexity. The consultant must be a US permanent resident or citizen.
Please send cover letter, CV, and consultant rate expectations to careers@collaborationspharma.com.
Collaborations Pharmaceuticals, Inc.® is a privately owned company that performs research and development on innovative therapeutics for multiple rare and neglected infectious diseases. We develop and apply our artificial intelligence (AI) software to aid in drug discovery and toxicology assessment as well as to identify and translate early preclinical to clinical stage assets. Our software can also be used to design new molecules with desired properties. This software can be used by pharmaceutical, consumer product, as well as other companies that require chemistry.
