VP CMC
VP CMC
Job ID: PR/045283
- Job Type
- Permanent
- Salary
- USD $330,000
Vice President, CMC
Job Type: Permanent
Location: United States (EST) – Hybrid Remote
Salary: $330K - $385K + Bonus + Stocks + Benefits
This position is with a small dynamic biopharma who specialize in Peptide based Therapeutics. Their lead asset is now progressing to Phase 3, this position will be to support the strategy and launch path from Phase 2 > 3 > commercialization.
You will lead internal / external teams in drug substance and product manufacturing and development. This role oversees all aspects of manufacturing, assay development, and supply chain to ensure efficient, cost-effective, and high-quality product development.
• Oversee integration of manufacturing, assay, auto-injector development, supply chain, and related functions to meet company goals.
• Manage relationships with external contractors to ensure timely, high-quality, and compliant program delivery.
• Forecast short- and long-term product development budgets.
• Communicate manufacturing strategy and progress to the Chief Scientific Officer.
• Collaborate with Quality, Clinical, and Regulatory teams to align activities company-wide.
• Ensure all work complies with SOPs and company safety policies.
Requirements:
• 20+ years in process development, GMP manufacturing, and assay development
• 7+ years specifically in Peptide CMC
• Recent experience of taking assets from Phase 2 to Phase 3
• Minimum 5 years supervisory experience
Please reach out to David.fearnley@skillsalliance.com or call +1 917 692-1913 for further details.
Job Type: Permanent
Location: United States (EST) – Hybrid Remote
Salary: $330K - $385K + Bonus + Stocks + Benefits
This position is with a small dynamic biopharma who specialize in Peptide based Therapeutics. Their lead asset is now progressing to Phase 3, this position will be to support the strategy and launch path from Phase 2 > 3 > commercialization.
You will lead internal / external teams in drug substance and product manufacturing and development. This role oversees all aspects of manufacturing, assay development, and supply chain to ensure efficient, cost-effective, and high-quality product development.
• Oversee integration of manufacturing, assay, auto-injector development, supply chain, and related functions to meet company goals.
• Manage relationships with external contractors to ensure timely, high-quality, and compliant program delivery.
• Forecast short- and long-term product development budgets.
• Communicate manufacturing strategy and progress to the Chief Scientific Officer.
• Collaborate with Quality, Clinical, and Regulatory teams to align activities company-wide.
• Ensure all work complies with SOPs and company safety policies.
Requirements:
• 20+ years in process development, GMP manufacturing, and assay development
• 7+ years specifically in Peptide CMC
• Recent experience of taking assets from Phase 2 to Phase 3
• Minimum 5 years supervisory experience
Please reach out to David.fearnley@skillsalliance.com or call +1 917 692-1913 for further details.