Join a dynamic biotech organization as a QC Specialist - Incoming Goods for a 6-month full-time assignment. You'll be crucial in ensuring GMP compliance and maintaining ERP system accuracy while driving process improvements. This role is perfect for proactive professionals who thrive in cross-functional collaboration and operational excellence. Be part of a team that values consultants as equal contributors, empowering you to take ownership in a quality-driven environment. Read on to discover what challenges await you.

Over het bedrijf

Panda International

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We are seeking a QC Specialist – Incoming Goods to support the quality control operations of raw materials and sample management for a 6-month, full-time contractor assignment. Based onsite in the Leiden region, you’ll play a key role in ensuring GMP compliance and maintaining ERP system data accuracy while contributing to process improvement initiatives.

This role is ideal for a proactive professional with experience in GMP environments who enjoys cross-functional collaboration and operational excellence.

Company Description:
You’ll be joining a fast-paced biotech organization at the forefront of developing advanced cell therapies, biologics, and small molecules for high unmet medical needs. Operating across Europe and the U.S., the company leverages decentralized manufacturing and cutting-edge science to accelerate patient impact. Consultants are valued as equal contributors and are empowered to take ownership of critical activities in a collaborative, quality-driven environment.

Essential Requirements:

1–2 years of experience in the pharmaceutical or biotech industry
Experience working under GMP guidelines, especially related to raw materials
Hands-on involvement in raw material release, sampling, and compliance documentation
Bachelor’s degree in Life Sciences, Biotechnology, or related discipline
Ability to manage ERP system master data, enforce documentation standards, and support deviation/CAPA processes
Strong interpersonal and communication skills
Self-driven and solution-oriented with a commitment to quality

Desirable Requirements:

Working knowledge of SAP and tools such as Excel and SharePoint
Experience with sample management processes and inventory control
Prior exposure to change controls, specification updates, and QC documentation systems
Collaborative and service-minded mindset with the ability to work across departments

Additional Insights:

Start Date: Preferably September
Duration: 6-month assignment
Employment Type: Full-time Consultant
Location: Netherlands – onsite presence required (Leiden region preferred)

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Quality Control Medewerker Leiden Fulltime Leiden Tijdelijk contract Leiden Leiden Provincie Zuid-Holland Quality Control Medewerker Salaris Quality Control Medewerker

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