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# Automation Specialist Pharma (CSV-QA)

- **Company:** Talentmark
- **Location:** Leiden, Netherlands
- **Experience:** Experienced
- **Contract:** Temporary contract
- **Skills:** Computer Programming, Data Integrity, Laboratory Information Management Systems, Software Engineering, System Testing, Information Technology, Trackwise, GXP
- **Published:** October 23, 2026
- **Apply:** https://www.careerjet.nl/job/nl8b9ef62b81f5fdb04736098f4a757c7d/eaa

## About the Role

* A bachelor's degree (HBO) in Life Sciences, Computer Science or equivalent experience in a similar role.
 * At least 2 years of pharmaceutical industry experience with GMP and automation responsibilities, plus knowledge of QC compliance and FDA/EMA guidelines.
 * Hands-on software development/programming experience and computerised system validation experience in a GxP environment.
 * An analytical, proactive approach, strong documentation and planning skills, and the ability to work independently and across teams.
 * Excellent written and spoken English; Dutch is a plus.
 * Must reside within 60 km of Leiden.
 * Candidates who do not have a valid work permit for the Netherlands will not be considered.

Preference: Laboratory experience, familiarity with systems such as Empower, LIMS or TrackWise, TECAN robotics, GAMP5, 21 CFR Part 11 or Lean/Six Sigma.
Ready to put your technical and investigative skills to work? Apply now and help build reliable, compliant laboratory operations.

## Description

Turn your automation expertise into reliable laboratory solutions. In this role, you'll combine hands-on technical work with non-conformance investigations to strengthen data integrity, resolve issues and keep pharmaceutical QC laboratories GMP-compliant.
What you'll do

 * Lead non-conformance investigations, identify root causes and drive corrective and preventive actions (CAPA).
 * Implement, maintain and troubleshoot laboratory systems, from analytical instruments to platforms connected to LIMS.
 * Safeguard data integrity, maintain technical documentation and support GMP and 21 CFR Part 11 compliance.
 * Collaborate across teams on automation projects, continuous improvement and audit readiness.