Global Head ADQC Gene Therapy
Genentech
Biotechnology
Philadelphia, PA - USA
Manager / Team Leader
Experteer Overview
In this role you drive the global Analytical Development and Quality Control strategy for the gene therapy portfolio, guiding science-driven, risk-based analytics from candidate nomination to commercialization. You shape the ADQC organization, set governance and external partnerships, and push state-of-the-art methods for viral vectors and nucleic acids. You will influence the broader gene therapy landscape and partner with regulatory bodies to advance industry benchmarks. This is a high-impact, cross-functional leadership position.
Compensation / Benefits
- relocation benefits
- discretionary annual bonus
- competitive salary
- comprehensive benefits package
- work with cross-functional teams
- potential for bonus based on performance
Responsibilities
- Define and evolve the global ADQC roadmap for the full gene therapy portfolio
- Shape the global organizational design and operating model for ADQC
- Direct end-to-end analytical strategies, method development, and QC testing across global sites
- Lead innovation in analytical capabilities for viral vectors and nucleic acids
- Serve as the authoritative voice for ADQC in project teams and governance boards; collaborate with Research, Regulatory, QA, MSAT, and Manufacturing to ensure CMC alignment
- Influence external stakeholders and regulators to set next-generation industry benchmarks
Key requirements
- Advanced degree (Master’s or PhD) in Chemistry, Biochemistry, Biology, or related discipline with strong analytical techniques (e.g., HPLC, Mass Spec, Genomics)
- 20+ years in research or biotech, with progressive responsibility in Gene Therapy or Biologics analytical development
- At least 10 years in supervisory or lead roles
- Deep technical expertise in viral vectors and nucleic acid formats; experience across AAVs, plasmids, and RNAs
- Proven track record in lifecycle leadership from development to commercialization
- Strong leadership; ability to build and empower global, cross-functional teams
- Familiarity with GMP and CMC requirements and regulatory expectations
Description
In this role you drive the global Analytical Development and Quality Control strategy for the gene therapy portfolio, guiding science-driven…
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