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Director Analytical Development Jobs in San Ramon, CA

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Director Analytical Development information

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$99.5K

$213.9K

$321.3K

How much do director analytical development jobs pay per year?

As of Aug 28, 2026, the average yearly pay for director analytical development in San Ramon, CA is $213,906.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,000.00 and $278,300.00 per year, depending on experience, location, and employer.

What is a director analytical development?

A Director of Analytical Development oversees the strategy, development, and implementation of analytical methods to support product development and manufacturing. They lead a team of scientists, ensure regulatory compliance, and collaborate with cross-functional teams to optimize processes. Their role includes troubleshooting analytical issues, validating methods, and contributing to regulatory submissions. This position is critical in maintaining product quality and ensuring data-driven decision-making in pharmaceutical, biotechnology, or related industries.

What are the typical daily responsibilities of a director analytical development?

A Director Analytical Development typically oversees the design, implementation, and optimization of analytical methods to support product development and quality control. This involves leading a team of scientists, ensuring projects meet regulatory requirements, troubleshooting technical challenges, and collaborating closely with cross-functional groups such as R&D, quality assurance, and manufacturing. Daily tasks often include reviewing analytical data and reports, planning project timelines, and making strategic decisions to align with organizational objectives. The role requires balancing hands-on scientific guidance with high-level management to drive innovation and efficiency within the analytical function.

What are the key skills and qualifications needed to thrive in the director analytical development position, and why are they important?

To thrive as a Director Analytical Development, you generally need an advanced degree in chemistry, biochemistry, or a related scientific field, along with substantial experience in analytical method development and validation, and team leadership. Familiarity with laboratory information management systems (LIMS), chromatographic and spectroscopic instrumentation, and regulatory guidelines such as ICH, FDA, and GMP is crucial. Excellent project management, strategic thinking, and interpersonal communication are standout soft skills for this position. These competencies enable effective oversight of complex analytical projects, ensure regulatory compliance, and foster team collaboration in a fast-paced R&D environment.

What are popular job titles related to Director Analytical Development jobs in San Ramon, CA?

For Director Analytical Development jobs in San Ramon, CA, the most frequently searched job titles are:

What job categories do people searching Director Analytical Development jobs in San Ramon, CA look for?

The top searched job categories for Director Analytical Development jobs in San Ramon, CA are:

What cities near San Ramon, CA are hiring for Director Analytical Development jobs?

Cities near San Ramon, CA with the most Director Analytical Development job openings:

Director, Analytical Development

Redwood City, CA • Hybrid

Full-time

Re-posted 17 days ago


Job description

The Opportunity:

  • Provide strategic and organizational leadership for analytical development activities supporting small molecule API and drug product development, including oversight of phase appropriate control strategies, specification setting, analytical lifecycle management, and overall CMC analytical strategy.

  • Lead and oversee analytical development execution across internal and external teams to support the development, characterization, and manufacturing of API and drug product, while actively contributing to cross functional PDM project teams.

  • Provide strategic guidance and oversight for regulatory submission activities, including authoring and review Quality sections of regulatory submissions, and leading responses to regulatory queries.

  • Establish and drive analytical strategies, technology selection, and operational execution through effective management of CDMOs, CROs, and contract laboratories, with accountability for quality, timelines, risk management, and delivery.

  • Provide leadership oversight for preparation, review, and approval of analytical protocols, reports, specifications, investigations, and technical documentation to ensure scientific excellence, regulatory compliance, and inspection readiness.

  • Build strong cross functional partnerships and influence across Drug Product, Drug Substance, Regulatory Affairs, QA, Project Management, Medicinal Chemistry, DMPK, Toxicology and senior leadership teams to drive strategic decision making and achievement of program and organizational goals.

Required Education, Experience and Skills:

  • PhD or Masters in related field.

  • 10+ years of progressive leadership experience in analytical development within the pharmaceutical or biotechnology industry.

  • Proven ability to lead cross functional teams, influence organizational decision making, and drive execution of complex development strategies in a matrix environment.

  • Extensive strategic and operational leadership experience overseeing analytical activities across small molecule drug development, with strong preference for late phase development, regulatory approval, and commercialization readiness.

  • Excellent communication, collaboration, people leadership, and stakeholder management skills.

  • Deep understanding of CMC strategies and analytical enablement for small molecule development programs.

  • Demonstrated leadership experience managing external partners, including CROs and CDMOs, to ensure high quality deliverables and program execution.

  • Strong knowledge of global regulatory requirements and experience supporting regulatory submissions, including INDs, IMPDs, NDAs, and/or MAAs.

  • In-depth understanding of ICH guidelines, GMP regulations, and current industry best practices related to analytical development and quality.

  • Strong strategic thinking and innovation mindset with the ability to independently evaluate complex issues, identify risks, and implement effective solutions.

  • Ability to prioritize and lead multiple initiatives in a fast paced, dynamic, and highly collaborative environment.

 Preferred Skills:

  • PhD preferred (minimum MS) in Analytical Chemistry, Organic Chemistry, or a related scientific discipline. #LI-Hybrid #LI-CT1