Spyre Therapeutics is a clinical-stage biotechnology company pioneering long-acting antibodies and antibody combinations to redefine the standard of care for inflammatory bowel disease (“IBD”) and rheumatic diseases.
Requirements
- Bachelor’s degree or advanced degree in chemical engineering, biochemical engineering, chemistry, biotechnology or related field, or commensurate years of education and experience
- Minimum 8 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 oversight 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
Benefits
- Market competitive compensation and benefits package, including base 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 complex problems and build relationships