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Equipment Specialist Oegstgeest Panda International

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior
  • Engels (taal)

Aanbod

  • Tijdelijk contract
 

Vacature in het kort

Oegstgeest
Join an innovative biotech organization as an Equipment & Systems Specialist (Consultant) for a 6-month full-time assignment. Lead the charge in equipment lifecycle management and compliance across a decentralized manufacturing network. You'll coordinate qualification and maintenance, support audits, and ensure system integrity while crafting GMP-compliant documentation. Be part of a purpose-driven team advancing life-saving treatments in a collaborative environment. Read on to discover why this job might be perfect for you.
 

Over het bedrijf

Panda International
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Volledige vacaturetekst

We are seeking an experienced Equipment & Systems Specialist (Consultant) to lead equipment lifecycle management and compliance activities across a decentralized manufacturing network. This is a 6-month full-time assignment, ideally based in the Leiden region or with the ability to travel to site.

You will play a key role in coordinating qualification and maintenance efforts, supporting audits and system integrity, and writing essential GMP-compliant documentation. This role is critical to maintaining operational readiness and data integrity for QC and manufacturing equipment supporting advanced therapy programs.

Company Description:
This innovative biotech organization is transforming the future of healthcare through scientific excellence and decentralized cell therapy manufacturing. With a strong pipeline in immunology and oncology, the company focuses on unmet medical needs and pushes the boundaries of what's possible. You’ll join a collaborative, purpose-driven environment where your work directly supports life-saving treatments and cutting-edge manufacturing.

Essential Requirements:

  • Experience managing the full equipment lifecycle, including qualification and maintenance coordination, ideally in a QC and manufacturing setting

  • Hands-on experience writing URS, IQs, OQs, PQs

  • Background in a GMP-regulated environment, preferably involving ATMPs (Advanced Therapy Medicinal Products)

  • BSc in Life Sciences, Biotechnology, or a related field

  • Excellent communication skills and a proactive, quality-first mindset

  • Ability to manage shifting priorities with independence and accountability

  • Fluent in English

Desirable Requirements:

  • Experience with Computer System Validation (CSV) is a strong plus

  • Familiarity with ICH guidelines and regulatory expectations for ATMPs

  • Previous experience supporting multi-site equipment compliance or technical transfers

Additional Insights:

  • Start Date: ASAP

  • Duration: 6 months

  • Employment Type: Full-time Consultant

  • Location: Netherlands (Leiden region preferred or willingness to travel to Leiden office)

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