Quality Inspection Specialist, Haarlem, Noord-Holland

Location: Haarlem, Noord-Holland  |  Sector: Pharmaceuticals  |  Start Date: 12/10/2025  |  Job ref: 56845

The Company
Our client is a globally recognized organization operating within regulated, high-quality manufacturing environments. With a strong focus on science, safety, and innovation, the company is dedicated to delivering reliable products that positively impact public health. Its operations combine advanced technology, strict compliance standards, and a culture built on precision, collaboration, and continuous improvement.

Role Description
As a Quality Inspection Specialist, you will play a key role in ensuring the accuracy and compliance of packaging components used in critical production processes. You will perform a variety of tests, checks, and administrative tasks that contribute directly to product quality and regulatory compliance. Working under well-defined procedures and guidelines, you will help safeguard consistency, reliability, and operational excellence across the QC function.
This position is well-suited for detail-oriented professionals who thrive in structured environments and enjoy hands-on quality work.


Responsibilities
- Perform inspections and tests on primary and secondary packaging components according to established procedures, GMP expectations, and applicable regulations.
- Utilize text verification tools (including Braille measurement systems) to ensure conformity to specifications.
- Conduct repetitive measurement activities such as weighing and sizing components.
- Interpret results against defined standards and document all findings accurately.
- Work with various digital systems, including enterprise-quality or production-related applications.
- Evaluate deviations or anomalous findings and escalate appropriately.
- Review administrative tasks and colleagues’ results to ensure accuracy, completeness, and compliance with quality guidelines.


Requirements
- Completed vocational education (MBO level 2 or 3).
- Preferably some experience in highly regulated environments such as pharmaceutical, medical device, food, or hospital settings.
- GMP knowledge is an advantage, but not required.
- Strong attention to detail, patience, and the ability to perform repetitive tasks with focus.
- Effective communication skills in Dutch (verbal and written) and sufficient proficiency in English.
- Enjoys collaboration and contributes positively to team efficiency.


Other Information
If you're seeking a stable and meaningful opportunity within a quality-focused environment, this role may be an excellent next step.

56845

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About us

Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.

SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.

Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.

Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.