Director, Quality Control
About The Position
About Jade Biosciences Jade Biosciences is focused on developing innovative, best-in-class therapies to address critical unmet needs in autoimmune diseases. Our lead candidate, JADE101, is designed to inhibit the cytokine APRIL (A Proliferation-Inducing Ligand) and is being developed for the treatment of immunoglobulin A nephropathy ( IgAN ), a chronic kidney disease that can impair kidney function over time. JADE101 aims to reduce harmful IgA antibodies, lower proteinuria (a key marker of kidney damage), and preserve long-term kidney function. A Phase 1 healthy-volunteer study of JADE101 is ongoing, with interim, biomarker-rich data expected in the first half of 2026. Jade’s pipeline also includes a second development candidate, JADE201, and an undisclosed antibody discovery program, JADE-003, both currently in preclinical development. For more information, visit JadeBiosciences.com and follow us on LinkedIn . Role Overview The Director, Quality Control will lead critical Quality Control activities to support Jade’s product pipeline across various stages of development. The Director will manage analytical method life cycle including method development, qualification, testing, transfer and validation as phase appropriate. This individual will work very closely with internal stakeholders and external CDMO partners and will be responsible for developing and executing product release testing, stability study and product shelf-life strategy while ensuring full quality compliance with regulatory requirements and internal quality systems.
Requirements
- MS or PhD degree in Chemistry, Biology, Biochemistry, or related field with 10+ years of related experience
- 7+ years in Quality Control management for director level within the biotech or pharmaceutical industry
- A strong quality compliance and collaborative mindset, and ability to thrive in a fast paced working environment
- Strong knowledge of cGMP, FDA, EMA, and ICH regulations
- Strong experience in analytical method development including phase appropriate method qualification, transfer and validations from early to late phase development including BLA filing
- Experience with common analytical techniques such as common compendial methods, HPLC/UPLC, CE-SDS, ELISA, and cell-based assays for biologics development
- Proven leadership in managing internal QC operations or external CDMOs
- Excellent communication, organizational, and problem-solving skills
Responsibilities
- Work with both internal (other CMC functions, Quality Assurance, Regulatory and other key stakeholders) and external CDMO partners to develop and implement QC strategies appropriate for different phases of development programs
- Oversee batch release and stability testing, method development, qualification, transfer and validation activities at and cross CDMOs
- Develop product specifications and oversee product in-process, release, and stability testing strategy and execution in compliance with both cGMP and ICH guidance and internal quality standard
- Work with Quality Assurance to create and manage QC documentation including SOPs, protocols, and technical reports
- Collaborate cross-functionally with other CMC functions, QA and Regulatory to support tech transfers and lifecycle management, regulatory filing and interactions etc.
- Manage CDMO relationships to ensure compliance with quality standards, timely deliverables, and effective communication
- Review and approve CDMO generated data, investigations, and documentation
- Ensure timely investigation and resolution of OOS results, deviations, and CAPAs
- Serve as QC subject matter expert during regulatory inspections and audits
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What This Job Offers
Job Type
Full-time
Career Level
Director
Education Level
Ph.D. or professional degree
Number of Employees
11-50 employees
