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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

QA Specialist 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHoofddorp, NetherlandsNo salary listed

About the Job

Requirements

  • Strong working knowledge of Good Manufacturing Practices and/or Good Laboratory Practices.
  • Experience in deviation and corrective and preventive action management, impact assessments, and root cause investigations.
  • Strong technical writing, reporting, and documentation review skills.
  • Effective verbal communication, interpersonal, and stakeholder-management skills.
  • Proficiency in Microsoft Office applications.
  • A Bachelor's degree (BS/BA) and at least 3 years of relevant experience in a Good Manufacturing Practice-regulated environment, or a Master's degree (MS) and at least 1 year of relevant experience.

Responsibilities

  • Perform a variety of quality assurance activities to ensure compliance with applicable regulatory requirements and company procedures.
  • Maintain programs and processes to ensure high-quality products and compliance with current Good Manufacturing Practices and Good Laboratory Practices.
  • Provide front-line quality assurance support to escalations, ensuring timely actions and clear resolution paths.
  • Contribute to quality-on-the-floor processes, including shop-floor rounds and real-time quality assurance support.
  • Perform quality assurance review and approval of deviations and corrective and preventive actions.
  • Conduct or coordinate investigations and corrective and preventive action recommendations related to manufactured products.
  • Identify and report deviations from approved processes and procedures to senior colleagues.
  • Participate in developing Standard Operating Procedures to ensure quality objectives are met.
  • Exercise judgment within well-defined procedures and practices to determine appropriate action; identify problems and generate alternatives and recommendations within defined processes.
  • Work directly with operating entities to ensure inspections and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications.
  • Mentor junior staff and take on some task-management responsibility.
  • Contribute to quality assurance projects and participate in cross-functional teams.
  • Coordinate the planning, organization, and implementation of projects within specified objectives.
  • Work on complex, non-routine projects or assignments requiring analysis of identifiable factors.

Desired Qualifications

  • Prior experience in the pharmaceutical or biopharmaceutical industry.

About the Company

Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Gilead Sciences is a biopharmaceutical company that discovers, develops and sells medicines for HIV, viral hepatitis and other liver diseases, cancer and inflammatory conditions. Its HIV business covers both treatment, led by the once-daily pill Biktarvy, and prevention, including Descovy and Yeztugo, a lenacapavir injection given twice a year. In cancer, its Kite unit makes CAR T-cell therapies from patients' own immune cells, and Trodelvy is an antibody-drug conjugate for breast cancer. Gilead earns revenue by selling its drugs to wholesalers, specialty pharmacies, hospitals and governments worldwide after regulatory approval. The company was founded in 1987 and is headquartered in Foster City, California.

Company size
10,001+
Company stage
IPO
Headquarters
Foster City, CA
Founded
1987

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