E

Exelixis

Biopharmaceutical oncology company developing cancer therapies

Operations QA Manager - Commercial

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 7 years of related experience, an MS/MA degree in a related discipline and a minimum of 5 years of related experience, a PhD in a related discipline and 0 or more years of related experience, or an equivalent combination of education and experience.
  • Experience in the biotech or pharmaceutical industry is required.
  • Working knowledge of commercial and clinical manufacturing and quality processes, including US and EU regulations affecting the pharmaceutical industry.
  • Extensive experience in a virtual manufacturing environment or a relevant industry or profession.
  • Ability to develop technical solutions to complex problems and identify and implement methods, techniques, procedures, and evaluation criteria to achieve results.
  • Ability to interpret, execute, and recommend modifications to companywide policies or divisional programs.
  • Complete understanding and wide application of technical principles, theories, concepts, and techniques.
  • Attention to detail when using a PC, reviewing documents, and editing or proofreading documents.
  • Proficiency in Word, Excel, and PowerPoint.
  • Strong analytical and business communication skills, including verbal, written, and presentation communication skills.

Responsibilities

  • Provide QA oversight of end-to-end, day-to-day GMP operations at contract manufacturing organizations that generate company products, including drug substance, drug product, intermediates, raw materials, packaging, and labeling.
  • Assess vendor processes, systems, and procedures to evaluate quality performance against established standards and regulatory requirements.
  • Review batch records and participate in partnerships and collaborations to identify, rapidly mitigate, and escalate product risks.
  • Develop, establish, and maintain QA programs, policies, and procedures to ensure GMP compliance of commercial and clinical trial material.
  • Perform record review and disposition activities for commercial and clinical trial material, including comprehensive QA assessment.
  • Coordinate investigations with vendors and interdepartmental teams to resolve potential product quality issues.
  • Oversee generation, review, and/or approval of internal and external documents used in GMP activities.
  • Support the QA Partner in managing vendors, contract facilities, and joint development collaborators for contracts, validation activities, change management, and other QA issues.
  • Support implementation of quality systems, including departmental and corporate procedures, to ensure compliance with GMPs.
  • Understand regulatory agency policies and guidance as they pertain to QA issues.
  • Assist in monitoring current and proposed quality and scientific issues and advise the supervisor on events affecting the company.
  • Support review of quality review and approval documents, including manufacturing, testing, and labeling and packaging batch records, and CMC documents submitted to regulatory agencies.
  • Author work instructions and standard operating procedures.
  • Guide successful completion of major programs, projects, and/or functions.

Desired Qualifications

  • Experience in CMO oversight.
  • Technical knowledge of small molecules, oral solid dosage forms, and biologics.
  • Familiarity with serialization.

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

Recently Posted Jobs

Explore more opportunities at Exelixis

See more jobs