Manager, Contract Manufacturing

Role Overview

We're looking for a Manager, Contract Manufacturing on the Logistics team to help us expand what's possible for patients with serious diseases. Reporting to the Director, Contract Manufacturing, you'll oversee outsourced production at Contract Manufacturing Organizations (CMOs) or third-party manufacturers (TPMs), ensuring on-time delivery, high quality, and cost-effective production of pharmaceutical drug substance, drug product, and primary packaging.

What You Will Do

In this role, you'll have the opportunity to oversee the routine execution of manufacturing operations, resolution of technical issues, as well as deviations and change controls for pharmaceutical products. You will collaborate with cross-functional teams, including, MS&T, Quality Assurance, Regulatory CMC, and CMOs to ensure robust and compliant production processes.

Why It Might Be a Fit

You have a Bachelor’s degree along with 5 years of experience in pharmaceutical manufacturing, supply chain, or pharmaceutical development. You are or you also have: Experience with commercial CMO operations, Strong background in Manufacturing of Oral Solid Dosage forms including spray drying, tableting, and encapsulation technology for pharmaceutical applications, Working knowledge of quality systems, validation principles, engineering design, and statistical process control fundamentals, Proven ability to identify, assess, and solve technical problems, Experience with GMP manufacturing, technology transfer, process scale-up, and validation, High energy, innovative “can do” attitude, Ability to work independently without the need for constant supervision, Strong interpersonal skills and the ability to work in a fast paced, multidisciplinary environment, Strong verbal and written communication skills.

Requirements

• Bachelor’s degree
• 5 years of experience in pharmaceutical manufacturing, supply chain, or pharmaceutical development
• Experience with commercial CMO operations
• Strong background in Manufacturing of Oral Solid Dosage forms including spray drying, tableting, and encapsulation technology for pharmaceutical applications
• Working knowledge of quality systems, validation principles, engineering design, and statistical process control fundamentals
• Proven ability to identify, assess, and solve technical problems
• Experience with GMP manufacturing, technology transfer, process scale-up, and validation
• High energy, innovative “can do” attitude
• Ability to work independently without the need for constant supervision
• Strong interpersonal skills and the ability to work in a fast paced, multidisciplinary environment
• Strong verbal and written communication skills

Benefits

• Comprehensive medical, dental, and vision coverage
• Mental health support
• Annual wellbeing reimbursement
• Employee Assistance Program (EAP)
• Generous paid time off policies
• Fertility and family-forming benefits
• Caregiver support
• Flexible work schedules
• 401(k) plan with a competitive company match
• Annual equity awards
• Employee Stock Purchase Plan (ESPP)
• Company-paid life and disability insurance
• Company Learning Institute
• Employee resource groups
• Service and recognition programs
• Meaningful opportunities to connect, volunteer, and give back