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Technical Specialist QC Leiden Panda International

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Gevraagd

  • Fulltime
  • Engels (taal)

Aanbod

  • Loondienst (tijdelijk)
 

Vacature in het kort

Leiden
Join a dynamic laboratory team as a Technical Specialist, focusing on medium and high-quality compliance issues, cGMP compliance, and supporting new product introductions. Be the Subject Matter Authority during audits and inquiries, while providing technical expertise for lab systems and processes. Lead deviation management, drive continuous improvement projects, and maintain safety and reliability in operations, all while fostering effective communication and building trusted relationships. Read on to discover how this opportunity can transform your career.
 

Over het bedrijf

Panda International
Bedrijfsprofiel
 

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Job Role: Technical Specialist – Laboratory
About the Role:
We are seeking an experienced Technical Specialist to join a dynamic laboratory team. This role focuses on handling medium and high-quality compliance issues, maintaining cGMP compliance, and supporting new product introductions and lab operations. You will act as the Subject Matter Authority during audits and inspections and provide technical expertise for laboratory systems and processes.

Key Responsibilities:

  • Lead deviation management, acting as investigator for non-conformances and coordinating corrective and preventive actions (CAPAs).
  • Create, review, and update laboratory documentation, including supporting documents for new product introductions (NPI).
  • Provide technical support to the lab and contribute to cross-functional projects and services.
  • Act as technical system owner for analytical equipment and lab systems.
  • Serve as Subject Matter Authority during audits and inspections.
  • Lead and drive continuous improvement projects.
  • Promote and demonstrate safety, compliance, and reliability in daily operations.
  • Communicate effectively and build trusted relationships with team members, supervisors, and customers.
Key Competencies:
  • Strong analytical thinking and technical problem-solving skills.
  • Proven ability to work independently and collaboratively with cross-functional teams.
  • Knowledge of GMP and cGMP compliance requirements.
  • Experience in microbiological techniques such as bioburden, endotoxin, and sterility testing is a plus.
  • Excellent communication and interpersonal skills.
  • Experience with laboratory systems and equipment.
Requirements:
  • Bachelor’s degree (HLO) or higher in Life Sciences, Molecular Biology, or comparable field.
  • Fluency in English (written and spoken).
  • 2–5 years of relevant laboratory or pharmaceutical experience.
Practical’s:
  • Location: Leiden, Netherlands
  • Duration: 12 months (fixed-term contract)
  • Start Date: ASAP
  • Work Model: Full-time, On-site
 Interested or know someone who might be?
Send your CV or inquiries to via de button "Solliciteer nu" op deze pagina. to apply or learn more.
 

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