Genentech

Senior / Principal Technical Development Leader

Genentech$169K — $361K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • B.S./M.S/Ph.D. in chemistry, pharmaceutics, chemical engineering or related field
  • 10-15+ years in pharmaceutical industry, especially as a CMC team leader
  • Strong technical knowledge of large molecule process/product development
  • Advanced understanding of drug development process
  • History of successful innovation and recognized thought leader in CMC/product development

Responsibilities

  • Lead TDTs through asset lifecycle ensuring scientific integrity of CMC strategy
  • Develop and execute multifaceted technology strategies for product success
  • Provide strategic insights ensuring customer focus in project deliverables
  • Design innovative strategies for licensure of new modalities and therapeutics
  • Represent Pharma Technical functions on asset/lifecycle teams
  • Oversee manufacturing and delivery of clinical supplies while managing costs
  • Serve as primary decision-maker for CMC development and investments

Benefits

  • Relocation benefits available
  • Discretionary annual bonus based on individual and company performance
  • Comprehensive health benefits
  • 401(k) plan with company match
  • Work-life balance and flexible work arrangements
Full Job Description
The Opportunity

The Technical Development Leader (TDL) is responsible for leading Technical Development Teams (TDTs) in crafting and driving Chemistry, Manufacturing, and Control (CMC) strategies for clinical drug candidates from early human trials through product launch. The TDL ensures successful achievement of TDT goals, effective risk mitigation, and seamless communication across teams and cross-functional collaborators. This role involves comprehensive project planning, scheduling, resourcing, and reporting.

This position requires proven ability to effectively lead teams and work in situations with a high degree of ambiguity and challenges and to solve complex problems/manage highly complex projects.

Major Duties and Responsibilities

  • Leadership: Lead scientific and technical teams throughout the asset lifecycle, from preclinical development to product launch, ensuring the scientific integrity of the CMC strategy.

  • Strategy Development & Execution: Develop and implement multifaceted technology strategies essential for product success, including manufacturing processes, drug product and device configurations, supply chains and regulatory submissions.

  • Enterprise-wide Perspective: Provide strategic insights and ensure customer focus in project deliverables; Maintain regular updates to project teams, senior management, and governance committees, ensuring transparent and informed decision-making.

  • Innovation: Design novel strategies for licensure of new modalities and efficient development of standard therapeutics, building new company capabilities.

  • Representation: Represent Pharma Technical functions on asset/lifecycle teams and partner with various team leaders to align CMC strategy with broader goals of the company. May act as a consultant to top executives.

  • Project Management: Oversee manufacturing and delivery of clinical supplies, manage CMC development costs, and ensure adherence to timelines, milestones and resource forecasts.   Anticipate and resolve issues, developing contingency and risk mitigation plans.

  • Decision-Making: Serve as the primary decision-maker for CMC development, investments, and risk management, employing effective decision-making processes.


Who You Are

The TDL role demands excellent communication, collaboration, strategic and critical thinking, decision-making, negotiating, and influencing skills, along with the ability to lead complex projects and solve intricate problems.

Required:

  • B.S./M.S/Ph.D. degree in chemistry, pharmaceutics, chemical engineering or related field

  • 10-15+ years of experience in the pharmaceutical industry, with prior experience as a CMC team leader and strong technical knowledge of large molecule process and product development.

  • Advanced understanding of the drug development process and a history of successful innovation, recognized as a thought leader in CMC/product development.

Preferred:

  • Program Management: Demonstrated ability to handle complex, cross-functional programs and innovate new ideas and approaches.  Ability to work proactively and think strategically.   Strong negotiation and decision-making skills. 

  • Collaboration: Effective collaborating with team members and senior management. Successful experience working with third parties.

  • Communication: Excellent verbal and written communication skills, with a history of influencing others in cross-functional areas.

The expected salary range for this position based on the primary location of South San Francisco, CA is $169,100 to $314,000 (Senior TDL) OR $194,900 to $361,900 (Principal TDL). Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.

Relocation benefits are available for this job posting.

About Genentech

Genentech is a biotechnology company that develops and manufactures drugs for the treatment of serious medical conditions. The company was founded in 1976 and is headquartered in South San Francisco, California. Genentech's products include treatments for cancer, multiple sclerosis, and other diseases. The company is a subsidiary of Roche, a Swiss pharmaceutical company. Genentech has been recognized for its innovative research and development, and has received numerous awards for its contributions to the biotechnology industry.
Learn more about Genentech
Size
14,000 employees
Industry
Founded
1976

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