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Kite Pharma

Develops engineered T cell cancer therapies

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

Kite Pharma

Develops engineered T cell cancer therapies

Kite Pharma develops cancer immunotherapies by engineering a patient’s own T cells to attack tumors. Its core product strategy centers on cell therapy where T cells are genetically modified to recognize cancer cells, expanded outside the body, and then infused back into the patient to destroy cancer. This approach differs from traditional drugs by using the immune system itself to fight cancer and by tailoring therapies to individual patients. Kite focuses on clinical trials and commercialization of approved therapies, often through partnerships and licensing with other pharmaceutical companies to reach patients worldwide. The company’s goal is to provide potentially lifesaving, durable cancer treatments and move toward a cure for cancer.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Santa Monica, CA
Founded
2009

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