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Exelixis

Biopharmaceutical oncology company developing cancer therapies

Associate Director - Stability Management

Regulatory & Quality (Life Sciences)Updated on Nov 10
Full-timeAlameda, CA, USA

About the Job

Requirements

  • A BS/BA degree in a related discipline and a minimum of eleven years of related experience, or an MS/MA degree in a related discipline and a minimum of nine years of related experience, or a PhD degree in a related discipline and a minimum of five years of related experience, or an equivalent combination of education and experience.
  • GMP experience is preferred for successful entry into the job.
  • Technical laboratory experience in small molecules and solid oral dosage is preferred.
  • Pharmaceutical industry experience is preferred.
  • Extensive experience in the relevant industry or profession and area of specialization.
  • Ability to use professional concepts and company objectives to resolve complex issues creatively and effectively.
  • Ability to identify and implement methods and procedures to achieve results.
  • Understanding and broad application of technical principles, theories, concepts, and techniques.
  • General knowledge of related disciplines.
  • Strong analytical and business communication skills.

Responsibilities

  • Establish and manage the stability group within the CMC department, including overall strategy and oversight of stability and reference standard programs for drug substance, drug product, and reference standards across commercial and clinical programs.
  • Establish stability policies and procedures, and establish and manage performance metrics internally and with contract manufacturing organizations (CMOs).
  • Oversee CMOs’ execution of stability studies and authoring of stability protocols, interim stability reports, and final stability reports.
  • Oversee direct reports from the stability group.
  • Establish stability policies and procedures.
  • Establish and manage performance metrics.
  • Manage activities related to commercial and clinical drug substance and drug product stability testing.
  • Write and review stability protocols according to International Council for Harmonisation (ICH) guidelines.
  • Manage and monitor contract laboratory stability testing to ensure adherence to schedules outlined in stability protocols.
  • Review stability data, including raw test data.
  • Trend and track stability data to determine drug product shelf life and retest dates according to ICH guidelines.
  • Investigate out-of-trend or out-of-specification results according to industry best practices.
  • Manage, chair, and present in regularly scheduled stability committee meetings.
  • Write final stability reports for completed stability studies.
  • Review and assess temperature excursions during storage or transportation.
  • Generate certificates of analysis and retest memos, set and justify specifications for release and stability testing, and manage regulatory document controls.
  • Supervise staff, including hiring, scheduling, assigning work, reviewing performance, and recommending salary increases, promotions, transfers, demotions, or terminations.
  • Provide direction to other individuals.

Desired Qualifications

  • GMP experience.
  • Technical laboratory experience in small molecules and solid oral dosage.
  • Experience in the pharmaceutical industry.

About the Company

Exelixis

Biopharmaceutical oncology company developing cancer therapies

Exelixis develops and commercializes medicines for cancer. Its products aim to treat advanced cancers, including renal cell carcinoma, by targeting multiple biological pathways and supporting combination regimens to achieve effective, tolerable, and durable responses. The company generates revenue from sales of approved therapies and strategic partnerships, backed by extensive research, clinical trials, and regulatory approvals to bring new drugs to market. Compared with peers, Exelixis focuses on a pipeline that combines multi-pathway targeting with combination therapies to improve patient outcomes. Its overall goal is to advance cancer treatment and offer patients better chances of remission through its ongoing drug development programs.

Company size
1,001-5,000
Company stage
IPO
Headquarters
San Francisco, CA
Founded
1994

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