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Galapagos is hiring a

Technical Support GMP Specialist - Contractor (6 months), Leiden

Leiden, Netherlands

Job description

Pleased to meet you, we are Galapagos , a biotechnology company with operations in Europe and the U.S. dedicated to developing transformational medicines for more years of life and quality of life.

We are in the business of changing lives. Focusing on high unmet medical needs, we synergize compelling science, technology, and collaborative approaches to create a deep pipeline of best-in-class small molecules, CAR-T therapies and biologics in oncology and immunology. With capabilities from lab to patient, including a decentralized CAR-T manufacturing network, we are committed to challenging the status quo and delivering results for our patients, employees and shareholders.


Scope of the role:

We are seeking a GMP Specialist consultant to join the EU Technical Support team, supporting the GMP activities around equipment and systems available at our decentralized sites . The GMP Specialist will be an ambassador for the overall GMP culture and is a hands-on subject matter expert in handling deviations, CAPAs and Continuous Improvement projects.

Your role:

  • Actively engage in fostering understanding to continuously improve the GMP awareness related to the Technical Support area and broader EU Technical Operations team.
  • Mentor colleagues in handling deviations and CAPAs.
  • Track the progress on deviations and CAPAs and document review/approval.
  • Keep oversight on the training assignments within the department.
  • Support root-cause investigations for deviations, determine corrective actions and support implementation of change controls.
  • Support and foster a culture of Continuous Improvement.
  • Closely collaborate with Quality Assurance and other departments.

The GMP Specialist consultant reports to the Head of EU Technical Support.


Job requirements

Who are you?

  • BSc/MSc in life sciences, biotechnology, engineering or related discipline , with at least 5 years relevant working experience
  • Extensive experience with GMP manufacturing, Quality Systems, cell & gene therapy processes, automated bioreactors and process validation.
  • Responsible for own projects while pursuing company goals in open collaboration.
  • Result-driven and can-do mindset, without compromising quality and compliance
  • Good interpersonal skills and written and spoken fluency in English
  • Team player and good communication


What's in it for you?
At Galapagos, we prioritize your continuous growth and development, fostering a culture of empowerment. Our employees are the driving force behind our mission to lead in pharmaceutical research and innovation.

We offer a competitive compensation package and a supportive work environment with strong focus on your health and well-being. Join us in our journey towards sustainability, as we strive to make a lasting impact on both the industry and the planet.

Galapagos is dedicated to ensuring equal employment opportunities. Our hiring decisions are based on merit, considering qualifications, skills, performance, and achievements. We strictly prohibit discrimination against any employee or job applicant based on personal characteristics that are unrelated to their job.

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