Quality control analyst

SIRE LIFE SCIENCES; Haarlem; On-site; EUR 50,000 - 67,000; Full time

Job summary

SIRE LIFE SCIENCES is seeking a detail-oriented QC Analyst to join its analytical team in Haarlem, Netherlands. You will perform GMP-regulated testing on raw materials, in-process samples, and finished products to support timely releases.

Responsibilities include in-process testing with UHPLC/HPLC/GC, environmental monitoring, and non-routine tests like stability studies. Strong English and GMP experience are preferred. Shift work is involved.

Qualifications

• Degree in Analytical Chemistry, Chemistry, Life Sciences, or related field (MLO or HLO).
• Willing to work rotating 24/5 shift including nights/evenings/mornings.
• Strong attention to detail and commitment to quality and compliance.
• Hands-on GMP environment experience preferred.
• Fluent in spoken and written English.
• Able to adapt to changing laboratory conditions.

Responsibilities

• Conduct in-process control tests using UHPLC, HPLC, GC, PSD and other chemical methods.
• Perform daily environmental monitoring (conductivity, TOC, wet chemical analyses).
• Execute non-routine tests such as finished product release and stability studies.
• Review, document and evaluate analytical results in compliance with GMP guidelines and 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.
• Utilize LabWare LIMS and Empower 3; support testing and documentation processes.

Skills

Attention to detail

Fluent English

Education

Analytical Chemistry or related field

Tools

LabWare LIMS

Empower 3

Job description

Company

A leading pharmaceutical manufacturing organization dedicated to producing high-quality medicines for patients worldwide. The company emphasizes strict adherence to GMP standards, continuous improvement, and innovation within their state-of-the-art laboratories.

Job Description

We are seeking a detail-oriented QC Analyst to join a dynamic analytical team. In this role, you 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.


• Utilize laboratory equipment and systems to support testing and documentation processes, with experience in LabWare LIMS and Empower 3 preferred.

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.

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