QC Sample Administrator

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and join a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.

Location/Division Specific Information

The Groningen site is a biopharmaceutical site that develops and manufactures pharmaceutical products for clinical trials (phase 1, 2, and 3) and commercial production. It serves multiple clients and produces a variety of products.

Discover Impactful Work

As a QC Sample Administrator, you will play a crucial role in ensuring the flawless execution of our cGMP production processes. Your work will directly contribute to the safety and efficiency of our pharmaceutical products, impacting patient care globally.

Job Description:

• Receipt and booking of a wide variety of samples in the Laboratory Information Management System (LIMS).
• Aliquoting bulk samples under controlled conditions.
• Assisting in sample shipments to test laboratories, customers, and other external parties.
• Control inventory of samples, back-ups, and retains within QC.
• Processing data of external test results.
• Writing and updating procedures, logbooks, and other documentation.
• Performance of inspections, sampling and analytical tests related to raw materials.

Keys to Success:

• Capability to work independently and in a team.
• Excellent communication and interpersonal skills.
• Strong organizational and planning abilities.
• High attention to detail and accuracy.

Education

• Laboratory education on MBO level (e.g., MLO analytical chemistry or equivalent experience).

Experience

• Relevant experience in a biopharmaceutical or analytical laboratory environment.
• Previous background in a cGMP setting is preferred.

Knowledge, Skills, Abilities

• Attitude that prioritizes quality.
• Reliable and accurate work ethic.
• Proficiency in English at MBO level for reading and writing.

Physical Requirements / Work Environment

This role requires working in a controlled laboratory environment, handling samples, and adhering strictly to safety and quality protocols.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. We offer employment with an innovative, forward-thinking organization, and outstanding career and development prospects in an exciting company culture that stands for integrity, intensity, involvement, and innovation!