Stratacuity: Proven Scientific Placement
Associate Director CMC, Drug Product 2064423
Stratacuity: Proven Scientific Placement, Boston, Massachusetts, us, 02298
Associate Director CMC, Drug Product 2064423
Job Overview : Seeking a Manager/Senior Manager, CMC, Drug Product to oversee small molecule drug development, manage outsourced development activities, and handle cGMP manufacturing campaigns.
You can get further details about the nature of this opening, and what is expected from applicants, by reading the below. Primary Job Responsibilities: Lead CMC drug product projects, including development, optimization, and manufacturing at CDMOs. Direct process scale-ups and technology transfers ahead of commercial demand. Collaborate on refining development and testing methods with internal and external experts. Draft critical CMC drug product sections for regulatory submissions, ensuring compliance. Primary Job Requirements: PhD or MSc with extensive experience in chemistry or pharmaceutical sciences. 5+ years in pharma with expertise in solid dosage form development and cGMP manufacturing. Familiar with US, Canadian, and EU regulatory requirements; experienced in regulatory filings. Seniority level Mid-Senior level Employment type Full-time Job function Manufacturing, Science, and Research Industries Biotechnology Research and Pharmaceutical Manufacturing
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Job Overview : Seeking a Manager/Senior Manager, CMC, Drug Product to oversee small molecule drug development, manage outsourced development activities, and handle cGMP manufacturing campaigns.
You can get further details about the nature of this opening, and what is expected from applicants, by reading the below. Primary Job Responsibilities: Lead CMC drug product projects, including development, optimization, and manufacturing at CDMOs. Direct process scale-ups and technology transfers ahead of commercial demand. Collaborate on refining development and testing methods with internal and external experts. Draft critical CMC drug product sections for regulatory submissions, ensuring compliance. Primary Job Requirements: PhD or MSc with extensive experience in chemistry or pharmaceutical sciences. 5+ years in pharma with expertise in solid dosage form development and cGMP manufacturing. Familiar with US, Canadian, and EU regulatory requirements; experienced in regulatory filings. Seniority level Mid-Senior level Employment type Full-time Job function Manufacturing, Science, and Research Industries Biotechnology Research and Pharmaceutical Manufacturing
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