Director, Product Development

Alnylam Pharmaceuticals • Cambridge, MA

1d • $197,100 - $266,700 • Onsite

About The Position

The Director, Product Development (Process Sciences) will lead process development, optimization, scale-up, process characterization and pre-validation for all RNAi drug products at Alnylam. The successful candidate will work closely with cross-functional teams and contract manufacturing organizations on drug product process development, characterization, process transfer and oversight of manufacturing processes.

Requirements

• Degree in pharmaceutical sciences, chemistry, chemical engineering, biochemical engineering
• Ph.D. or MS degree with 16+ years’ experience in pharmaceutical process development
• Demonstrated experience in process development and process validation of sterile drug products and dosage forms across multiple development projects including process transfer and management of cGMP contract manufacturing.
• Demonstrated management experience of successful drug product process development teams
• Experience working in close collaboration with technical, regulatory, quality, clinical, project management, legal, finance, and supply chain functions in a cGMP operational environment
• Experience in preparing regulatory documents including briefing documents for regulatory meetings, INDs, and NDAs
• In-depth understanding and hands-on experience in drug product formulation, process development and characterization
• Hands-on experience in analytical methods for characterization of drug products and processes
• Excellent leadership, organizational and communication skills
• Demonstrated strong operational execution and problem-solving skills
• Desire to work in a fast-paced, deadline-driven environment
• If employed in the U.S., being fully vaccinated against COVID-19 as defined by the Centers for Disease Control and Prevention (CDC) is required.

Responsibilities

• Lead drug product and process development, optimization, scale-up, characterization and pre-validation
• Author and review technical protocols and reports in support of late phase manufacture and process characterization activities
• Lead the preparation of the Drug Product section of regulatory filings and effectively represent the Drug Product function in interactions with regulatory authorities
• Contribute to strategic technical discussions and present progress at internal and external scientific meetings
• Effectively represent Drug Product development on cross-functional teams including internal program teams and externally with contract manufacturing and/or corporate partners
• Effectively integrate Drug Product activities with other CMC functions, including Drug Substance Development & Manufacturing, Analytical Development, Quality Assurance, and Regulatory Affairs
• Periodic travel to manufacturing and other partner sites is required

Benefits

• medical, dental, and vision coverage
• life and disability insurance
• a lifestyle reimbursement program
• flexible spending and health savings accounts
• a 401(k)with a generous company match
• paid time off
• wellness days
• holidays
• two company-wide recharge breaks
• generous family resources and leave

What This Job Offers

• Job Type: Full-time
• Career Level: Director