QC Technician

Company
Our client is a global leader in the production of generics and biopharmaceuticals. The aim is to develop new and innovative treatments and to offer patients more affordable solutions in different therapeutic areas. They have a complex global supply chain able to reach more than 60 counties.

Job Description
As a detail-oriented QC Analyst you will join a dynamic team and will perform GMP-regulated testing across various laboratory areas to ensure the quality of raw materials, in-process samples, and finished products. Your contributions will support timely product releases and manufacturing operations.

Responsibilities
- Conduct in-process control tests using techniques such as (U)HPLC, GC, PSD, and other chemical methods.
- Perform daily environmental monitoring, including conductivity, TOC, and wet chemical analyses.
- Execute non-routine tests like finished product release, stability studies, raw material testing, and validation-related analyses.
- Review, document, and evaluate analytical results in compliance with GMP guidelines and laboratory procedures.
- Support investigations, deviations, and troubleshooting for laboratory equipment and analytical issues.
- Maintain efficient laboratory workflows, facilitate sample flow, and contribute to continuous improvement initiatives.

Requirements
- Degree in Analytical Chemistry, Chemistry, Life Sciences, or a related field (MLO or HLO).
- Ability and willingness to work a rotating 24/5 shift schedule, including nights, evenings, and mornings.
- Strong attention to detail and a commitment to quality and compliance.
- Practical, solution-focused team player with hands-on experience in a GMP environment preferred.
- Fluent in spoken and written English.
- Adaptable to changing environment and laboratory conditions.

Other Information
If you are interested and want to apply, please submit your application via the apply button and contact me.

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