Associate Scientist II - Analytical Development

ZipRecruiter; California; On-site; USD 80,000 - 110,000; Full time

Job summary

A leading biopharmaceutical company is seeking an Associate Scientist II to join their Analytical Development team. This role involves driving analytical method readiness and performing cGMP lot release and stability testing for AAV-based gene therapies. Candidates should have a strong background in relevant scientific fields and experience in biotech settings.

Benefits

Flexible PTO

Career growth opportunities

Collaborative, data-driven environment

Learning and development resources

Competitive compensation and benefits

Qualifications

• 3+ years in biotech/pharma preferred.
• Strong documentation skills for GMP compliance.
• Self-motivated and detail-oriented.

Responsibilities

• Perform routine testing for GMP and non-GMP samples.
• Author test methods and qualification reports.
• Collaborate with Quality to maintain compliance.

Skills

Cell culture

Assays

Spectrophotometry

Documentation for GMP compliance

Team collaboration

Education

BS or MS in Biochemistry, Molecular Biology, Analytical Chemistry, Virology

Tools

ddPCR

qPCR

ELISA

Liquid handling platforms

Job description

Job Description

About GondolaBio

GondolaBio is a clinical-stage biopharmaceutical company focused on developing next-generation therapeutics for genetic diseases. Originally launched as BridgeBioX, a subsidiary of BridgeBio, GondolaBio secured $300M in private financing in 2024 and became an independent company within the BridgeBio ecosystem. The company aims to leverage cutting-edge biological research to create breakthrough medicines addressing high unmet needs across multiple therapeutic areas, including neurology, pulmonology, cardiology, nephrology, and endocrinology. Located on the Stanford Life Sciences campus, GondolaBio fosters a hybrid environment where top scientists collaborate with senior leadership and advisors, blending industry expertise with academic innovation.

About BridgeBio

BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines for genetic diseases and cancers with clear genetic drivers. Since its founding in 2015, it has built a portfolio of over 20 drug development programs across various therapeutic areas, with two approved drugs. The company focuses on translating scientific discoveries into medicines, with offices in the US and internationally. Learn more at https://bridgebio.com.

Who You Are

The Associate Scientist II will be part of the Analytical Development team within Technical Development and Operations. The role focuses on driving analytical method readiness and performing cGMP lot release and stability testing for AAV-based gene therapies. Responsibilities include technical document authoring, method optimization, transfer, and collaboration with Quality, Laboratory Operations, and Process Development teams to ensure compliance and support manufacturing.

Responsibilities

1. Perform routine testing for GMP and non-GMP samples supporting manufacturing and process development.
2. Execute qualification assays per protocols.
3. Author test methods and qualification reports.
4. Collaborate with Quality to maintain compliance of test methods and equipment.
5. Manage transfer of qualified assays to third-party testing sites.
6. Minimize assay turnaround times and prioritize work according to program needs.
7. Contribute to experiments characterizing recombinant AAV candidates.
8. Troubleshoot instrumentation and testing methods; support lab operations.
9. Ensure procedures and documentation meet quality and regulatory standards.
10. Document data and results in lab notebooks for GMP release, stability testing, and method qualification.

Qualifications and Skills

• BS or MS in Biochemistry, Molecular Biology, Analytical Chemistry, Virology, or related field; ideally 3+ years in biotech/pharma.
• Hands-on experience with cell culture, assays, spectrophotometry.
• Experience with ddPCR and qPCR; ELISA experience is a plus.
• Experience with liquid handling platforms is beneficial.
• Ability to operate methods and instruments independently.
• Strong documentation skills for GMP compliance.
• Self-motivated, organized, detail-oriented, with good communication skills.
• Team player able to collaborate across functions.
• Capable of working in a fast-paced environment with changing priorities.

What We Offer

• Patient Days and engagement with individuals living with conditions we aim to treat.
• A culture based on values: put patients first, think independently, transparency, science-driven.
• Decentralized structure enabling focus on science and patient impact.
• Ownership of your program and career path.
• Collaborative, data-driven environment.
• Learning and development resources.
• Competitive compensation and benefits.
• Flexible PTO, career growth opportunities, and cross-program involvement.