QC Analist

Talentmark Nederland B.V. · Amsterdam, Noord-Hollandapprox. The posting names no place; this is the employer's city.

Full-time#Chromatography & mass spec #GMP

Location: Amsterdam, Noord-Holland; The posting names no place; this is the employer's city.
Employment: Full-time
Salary: €39,600 a year
Posted: Today

About the job

QC Analist

• Laboratory

• Netherlands, Haarlem

• 26 oktober 2026

• Fulltime

• BH-71532

• €3300 per month

Are you passionate about laboratory work and eager to contribute to the quality and safety of pharmaceutical products? We are looking for a motivated Quality Control Technician III to join a dynamic, multidisciplinary analytical team in Haarlem.

In this role, you will work with a wide range of analytical techniques and contribute directly to the quality control of pharmaceutical products. From in-process control and environmental monitoring to raw material testing, product release and stability studies, your work will play an important part in ensuring reliable results and supporting the manufacturing operations.

You will join a professional, GMP-regulated laboratory environment where accuracy, collaboration and continuous improvement are essential. If you enjoy hands-on laboratory work, solving analytical challenges and working in a team that values quality, this is an excellent opportunity to put your expertise into practice.

The position is offered on an initial six-month contract, with the possibility of extension. You will work in a rotating 3-shift schedule, alternating between night, afternoon and morning shifts. The shift change is 24/5 based, so weekends are completely off. On top of that, you get a shift allowance of approximately 23%.

What will you do?

As a Quality Control Technician III, you will be responsible for a variety of analytical activities, including:

Performing in-process control testing using techniques such as (U)HPLC, GC, Particle Size Distribution (PSD) and other chemical methods;
Conducting daily environmental monitoring, including conductivity measurements, Total Organic Carbon (TOC) testing and wet chemical analyses;
Carrying out additional testing for finished product release, stability studies, raw materials and validation activities;
Evaluating, verifying and accurately documenting analytical results in accordance with GMP requirements and laboratory procedures;
Identifying and investigating deviations, supporting laboratory investigations and contributing to effective problem-solving;
Troubleshooting laboratory equipment and helping ensure reliable analytical performance;
Maintaining an efficient sample workflow and supporting the smooth operation of daily laboratory activities;
Contributing ideas and practical solutions to improve laboratory processes and maintain high quality standards.

What do you bring?

We are looking for a hands-on and quality-driven laboratory professional who takes pride in accurate work, enjoys tackling challenges and thrives in a collaborative environment.

In addition, you have

A completed MLO or HLO degree in Analytical Chemistry, Chemistry, Life Sciences or a related field;
Strong written and spoken English skills;
A keen eye for detail and a commitment to quality and compliance;
A proactive, practical and solution-oriented mindset;
The ability to work independently while contributing positively to a team;
Flexibility and the ability to adapt to a fast-paced laboratory and manufacturing environment;
The willingness and availability to work a rotating 24/5 shift schedule, including weekends and public holidays.

Nice to have

Hands-on experience with chromatographic techniques such as HPLC, UPLC or GC;
Familiarity with LabWare LIMS v7, Empower 3 or comparable laboratory systems;
Experience with deviation investigations, equipment troubleshooting or analytical problem-solving.
Previous experience in a GMP-regulated laboratory;

What can you expect?

Here you will have the opportunity to contribute to pharmaceutical quality within an international organisation dedicated to making medicines accessible to patients around the world.

You can expect

An initial six-month assignment, with the possibility of extension;
A salary of approximately €3,300 gross per month, excluding shift allowance;
A shift allowance of approximately 23%
Applicable shift allowances for the rotating schedule;
A professional, GMP-regulated laboratory environment;
Collaboration with an experienced, multidisciplinary analytical team;
Varied laboratory activities that allow you to apply and further develop your analytical skills;
The opportunity to make a meaningful contribution to product quality and the reliable release of medicines.

Interested?

Are you ready to put your analytical skills to work in the pharmaceutical industry and become part of a quality control team in Haarlem?

If you enjoy working with analytical techniques, solving problems and making a real contribution to product quality, we would love to hear from you!

Apply now or send us your CV. We look forward to telling you more about this opportunity!

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