QC Raw Materials Specialist/Group Leader Merrimack Pharmaceuticals
THIS JOB HAS EXPIRED Our work is founded on revolutionary drug discovery platform that integrates high throughput quantitative proteomics, computational biology, and chemical engineering into a singular capability to dissect complex biological systems with unparalleled productivity. Merrimack is organized by multi-disciplinary project teams focused on the development and delivery of a novel therapeutic and diagnostic.
The Quality Control Raw Materials Supervisor/Group Leader will be responsible for:
Participating in developing and maintaining a Raw Materials qualification program
Integrating qualification program with vendor / supplier approval processes in QA and Materials
Building an efficient sampling and testing program for all Raw Materials
Hands-on sampling and testing of chemical raw materials as appropriate
Establishing in-house testing for critical API?s and specialty chemicals (Lipids, SOS, TEA)
Managing outsourced testing as required
The Raw Materials program spans both protein biologic and liposomal pharmaceutical drugs. This position will be a key member of the Merrimack's drug development teams (Clinical Phase 1-3) and will work closely with manufacturing, QA, and materials management to bring up the levels of compliance and efficacy to support commercial manufacturing operations.
The position requires a BS or MS in biochemistry and 5-9+ years of experience in pharma/biotech QC and 0-4 years of supervisory experience. The ideal candidate should be experienced in Raw Materials sampling and testing and HPLC testing for proteins, lipids, and/or small molecules, with demonstrated experience in GMP quality systems. The candidate should have excellent team skills, effective organization and presentation skills; be reliable, motivated, have strong interpersonal communication skills (written and verbal) and be amenable to working in a team environment.
||One Kendall Square |
Building 700, Second Floor
Cambridge, MA 02139
THIS JOB HAS EXPIRED