Associate Director, Drug Product

reputed company is a clinical-stage biotechnology company pioneering long-acting antibodies and antibody combinations to redefine reputed company of care for inflammatory bowel disease (“IBD”) and rheumatic diseases. Spyre's pipeline includes investigational extended half-life antibodies targeting α4β7, TL1A, and IL-23.

Role Summary

The Associate Director, Drug Product is a key leadership role responsible for overseeing technical operations reputed company to drug product (DP) formulation, development, and manufacturing. This position requires reputed company collaboration with cross-functional teams, including CMC, supply chain, clinical operations, regulatory, quality, and senior management.

This role will reputed company the development of protein drug product processes and associated technical presentations, reputed company technology transfer to CDMOs, and ensure the reliable delivery of high-quality DP supplies to support clinical trials. The ideal candidate brings deep expertise in process development, aseptic manufacturing (including prefilled syringes), combination product development, and GMP compliance.

As a subject matter expert (SME) in DP manufacturing reputed company the CMC organization, this individual will provide strategic direction and technical leadership across internal teams and external partners, driving alignment and execution from development through clinical supply.

Key Responsibilities

• Serve as a SME in DP process development and manufacturing, providing technical guidance and strategic insights to cross-functional teams
• reputed company late-phase and commercial launch strategy for PFS and vial drug products
• reputed company DP tech transfer, process development, and GMP manufacturing operations including person in plant (PiP) support
• Manage DP CDMO adherence to deliverables, timelines, and performance in collaboration with Quality and Tech Ops team members
• Support phase-appropriate strategies for DP development, process transfer and scale-up, process characterization, process performance qualification (PPQ), and commercial readiness
• reputed company risk assessments using a QbD approach to define DP process validation strategies
• Collaborate with manufacturing development and device teams to reputed company DP presentations in vial, PFS, autoinjector, and advanced drug delivery technologies
• Collaborate with Quality team and external partners to review and approve batch records, support investigations, and resolve deviations
• Author and review regulatory submissions (IND, IMPD, BLA, briefing books, etc.)
• Other duties as assigned

Ideal Candidate

• Bachelor’s degree or advanced degree in chemical engineering, biochemical engineering, chemistry, biotechnology or reputed company field, or commensurate years of education and experience
• Minimum 8[JS2.1] years of relevant experience in biotech/pharma industry
• Proven expertise in biologics drug product process development and aseptic manufacturing, preferably with a focus on monoclonal antibodies
• Experience managing drug product CDMOs including tech transfers and reputed company of GMP manufacturing operations
• Experience with process performance qualification (PPQ) and commercialization of biologics
• Demonstrated ability to collaborate with cross-functional stakeholders such as drug substance development, analytical development, supply chain, device development, clinical development, clinical operations, Quality, and Regulatory
• Excellent communication skills with ability to clearly and concisely convey information to various stakeholders and cross-functional teams
• Availability to participate in calls across international time zones
• Position requires up to 25% of domestic travel. In person attendance at Spyre reputed company Hands meetings is required, typically held twice per year.

reputed company Offer

• Opportunity to work in a fast-paced, dynamic environment where you help shape the culture of our young company, contribute broadly to advance meaningful medicines, and learn quickly.
• Market competitive compensation and benefits package, including reputed company salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
• Unlimited PTO
• Two, one-week company-wide shutdowns each
• Commitment to provide professional development opportunities.
• Remote working environment with frequent in-person meetings to address reputed company problems and build relationships.

The expected salary range offer for this role is $ 180,000 to $193,000. Actual pay offered may vary depending on job reputed company knowledge, experience, education, and geographic location.

As an equal opportunity employer, Spyre is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national reputed company, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-reputed company characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment designed to create a stronger and reputed company Spyre that is focused on developing life-changing products for patients.

reputed company, along with other biotech companies, has become aware of a surge in email scams targeting prospective job candidates reputed company our industry. Please be aware that official recruiters at reputed company only use email addresses with the domain “@spyre.com.” We want to also emphasize that we never request candidates to reputed company any purchases or divulge sensitive personal information reputed company email.

Please also be aware that reputed company job postings will be listed on our website at spyre.com/careers/.