Quality Operations Associate, Boxmeer, Noord-Brabant

Location: Boxmeer, Noord-Brabant  |  Sector: Pharmaceuticals  |  Start Date: 12/5/2025  |  Job ref: 56793

The Company
Our client is a leading organization dedicated to advancing quality standards within the pharmaceutical and healthcare industry. Their Quality Operations Center of Excellence ensures manufacturing processes comply with strict cGMP requirements across production, testing, packaging and distribution.

Role Overview
Join the QA-IPT team within the Center of Excellence Quality Operations to support batch documentation review, cross-department coordination, and continuous improvement activities that keep manufacturing compliant and efficient.

Key Responsibilities
- Act as a core member of the QA-IPT team supporting daily QA activities.
- Conduct substantive review of batch documentation in collaboration with QA release specialists and senior QA associates.
- Communicate regularly with operational coaches to resolve documentation errors and non-conformances.
- Coordinate with other QA teams across sites to maintain harmonised processes.
- Liaise with planning to manage review timelines and ensure on-time processing.
- Track review progress and support the QA-IPT lead with workload control.
- Contribute to quality improvement initiatives and process optimisation efforts.
Requirements
- Degree (MBO/HBO/Bachelor/Master) in Life Sciences or related field, or equivalent experience (preferably 1–3+ years in QA/QC or manufacturing quality).
- Practical knowledge of GMP / cGMP (or demonstrable experience in regulated manufacturing).
- Strong attention to detail and good documentation/writing skills.
- Effective communication and stakeholder management skills.
- Able to work collaboratively within multi-disciplinary teams.
- Comfortable using digital systems (ERP/SAP and/or LIMS or QMS tools).
Experience specifically in batch review or QA-IPT style teams.
- Familiarity with TrackWise / MasterControl / LIMS.
- Prior experience in animal health, pharmaceutical or CMO environments.
- Exposure to continuous improvement methods (Lean / Six Sigma basics).

Apply Now
If you care about accuracy, compliance, and working with a team that keeps quality central to every step of manufacturing — apply today. We welcome candidates who are detail-oriented, collaborative, and ready to make an impact.

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

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