Manager, Quality Control

Insmed Incorporated • NJ Corporate Headquarters, NJ

2d • Onsite

About The Position

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: We're looking for a Manager, Quality Control (QC) on the Quality Control team to help us expand what's possible for patients with serious diseases. Reporting to the Associate Director, Quality Control, you'll independently lead and oversee all QC activities conducted at external contract laboratories for inhalation and small molecule drug substance, drug products, including raw materials, in-process, release, and stability testing. You will manage analytical projects, deviations, and investigations while ensuring all testing activities are compliant with cGMP, regulatory standards, and Insmed’s quality expectations.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
• 4 years of Quality Control experience within the biotech/pharmaceutical industry.
• Experience in analytical testing of inhalation and/or small molecule drug products.
• Strong understanding of cGMP regulations, ICH guidelines, and global compendial standards (USP/EP/JP).
• Experience with oversight of contract testing labs.
• Experience reviewing analytical data and technical documents such as CoAs, protocols, and regulatory submissions.
• Analytical and problem-solving skills, including participation in investigations and CAPA implementation.
• Effective communication and collaboration skills with ability to interface with internal teams and external partners.
• Time management and prioritization abilities, with attention to quality and compliance.

Nice To Haves

• Advanced degree (MS)
• Familiarity with combination products

Responsibilities

• Serve as a key interface between QC, Analytical Development, Regulatory Affairs, QA, and Supply Chain to support product development, lifecycle management, and regulatory submissions.
• Independently manage and provide technical oversight of QC testing conducted at contract laboratories for drug substances and drug products, with emphasis on inhalation dosage forms.
• Lead analytical project activities from initiation through completion, ensuring testing aligns with project timelines, quality expectations, and regulatory requirements.
• Review analytical data packages, protocols, test results, and reports for completeness, accuracy, and compliance with internal and external standards.
• Independently manage deviations, out-of-specification (OOS), out-of-trend (OOT) investigations, and change controls, including performing root cause analysis and implementing effective CAPAs.
• Support and drive analytical method implementation and troubleshooting related to APSD, MMAD, delivered dose, and particle size distribution testing.
• Ensure timely review and approval of Certificates of Analysis (CoAs), method validation/transfer protocols, and analytical methods from external labs to enable batch disposition.
• Lead the development and review of product specifications and justification documents for clinical and commercial programs.
• Author, review, and contribute to QC sections of regulatory submissions (INDs, NDAs) and prepare responses to regulatory agency inquiries.
• Monitor and evaluate contract laboratory performance metrics, providing technical guidance and escalating issues as needed.
• Drive continuous improvement initiatives within QC and external lab oversight processes.

Benefits

• Comprehensive medical, dental, and vision coverage and mental health support
• Annual wellbeing reimbursement
• Access to our Employee Assistance Program (EAP)
• Generous paid time off policies
• Fertility and family-forming benefits
• Caregiver support
• Flexible work schedules with purposeful in-person collaboration
• 401(k) plan with a competitive company match
• Annual equity awards
• Participation in our Employee Stock Purchase Plan (ESPP)
• Company-paid life and disability insurance
• Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities
• Employee resource groups
• Service and recognition programs
• Meaningful opportunities to connect, volunteer, and give back

What This Job Offers

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