Jade Biosciences is seeking an Associate Director, Quality Control to lead critical Quality Control functions supporting their product pipeline in a fully remote role.
About the Role
As the Associate Director, Quality Control, you will manage analytical method life cycle including development, qualification, transfer, and validation. You will collaborate with internal stakeholders and external CDMO partners to implement QC strategies, oversee product testing, and ensure compliance with regulatory requirements. Your responsibilities will also include managing CDMO relationships, reviewing documentation, and serving as a QC subject matter expert during inspections.
About You
Required:
Master's or advanced degree in Chemistry, Biology, Biochemistry, or related field with 10+ years of related experience (7+ years with PhD).
8+ years of experience in Quality Control management within the biotech or pharmaceutical industry.
Strong knowledge of cGMP, FDA, EMA, and ICH regulations.
Experience with analytical method life cycle management including method qualification, transfer, and validations.
Preferred:
Experience with common analytical techniques such as 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.
Benefits
Fully remote role with up to 20% domestic and/or international travel.
Competitive salary range of $170k–$190k based on experience and qualifications.
Jade Biosciences
Jade Biosciences is developing a pipeline of potentially best-in-class therapies aimed at transforming the standard of care for patients living with autoimmune diseases.
Company Size: 11-50 employeesBiotechnology Research