Scientist (I, II, III) - CMC
Our Client
Our client is a San Diego-based biopharma company developing cutting-edge monoclonal antibodies and antibody-drug conjugates for cancer and inflammatory diseases. Known for its innovative immuno-oncology approach and rapid growth through strategic acquisitions, it's been recognized as a top biotech startup and awarded Biopharmaceutical Company of the Year in California. If you're looking to bet on the future of cancer treatment, this is a fun one to watch.
Job Title: Scientist I / II / III - CMC
Location: San Diego, CA
Department: CMC / Biologics Development
Reports To: Director, CMC
Position Summary
Seeking motivated and detail-oriented Scientist I, II, and III candidates to support CMC activities for our pipeline of biologic therapeutics. The ideal candidate will contribute to the development, characterization, and manufacturing of monoclonal antibodies and ADCs from preclinical through clinical phases. Title will be commensurate with experience.
Key Responsibilities
Scientist I - Entry-Level
Assist in development of upstream and/or downstream processes for mAbs and ADCs
Support tech transfer, batch records, and documentation preparation
Conduct routine analytical testing (e.g., SDS-PAGE, SEC, ELISA)
Collaborate with external CDMOs to support CMC activities
Maintain accurate records in lab notebooks and internal systems
Scientist II - Mid-Level
Design and execute process development studies with minimal supervision
Lead specific workstreams within CMC projects
Analyze data, troubleshoot experiments, and present findings cross-functionally
Contribute to IND/IMPD filings by authoring and reviewing CMC sections
Oversee assay development and product characterization efforts
Scientist III - Senior-Level
Drive CMC strategy across multiple projects from early to late-stage development
Serve as technical lead for external partnerships and CDMOs
Guide junior staff and ensure scientific rigor in process development
Own and manage timelines, budgets, and quality for CMC deliverables
Represent CMC function in cross-functional meetings and regulatory discussions
Qualifications
Scientist I
BS/MS in Biochemistry, Chemical Engineering, or related field with 0-2 years of industry experience
Hands-on lab experience with biologics or protein purification preferred
Scientist II
MS/PhD in Biochemistry, Chemical Engineering, or related field with 3-6 years of industry experience
Proven track record in process development and analytical techniques
Scientist III
PhD with 5-8 years or MS with 8+ years of industry experience in biologics development
Deep expertise in CMC strategy, regulatory submissions, and manufacturing operations
Experience in leading tech transfers and managing CDMO collaborations