Associate Lab Specialist Quality Control – Transfers
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Associate Lab Specialist Quality Control – Transfers in Boxmeer (Noord-Brabant), biopharma, start 28-07-2026.
- Locatie
- Boxmeer
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Sluitingsdatum
- Eerste waarneming
- Opdrachtgever
- Global leader in biopharmaceuticals
Eisen
- Minimum of 5 years’ experience in a biological QC laboratory, preferably within GMP or GLP environments
- Familiarity with SAP, LIMS, and electronic QC data systems
- Proven expertise in transfer processes, data analysis, and root cause investigation
- Accurate, proactive, and solution-oriented with strong communication skills in English and Dutch
- HBO level education in (micro)biology, analytical chemistry, or similar field
Wensen
- Experience with change management and project leadership is advantageous
- Certified Yellow Belt or experienced with Lean/Six Sigma methodologies is a plus
Omschrijving
We are seeking a skilled Transfer Specialist to join the Quality Control team within our Animal Health division. This vital role involves managing the transfer of biological and analytical tests from R&D or other sites to our QC laboratories, ensuring high standards and timely execution. The successful candidate will play a key part in maintaining product quality and supporting ongoing quality improvements. Responsibilities: Serve as the expert on various biological and analytical test techniques; Manage and ensure the successful transfer of tests according to established transfer methodologies, including new R&D methods and existing tests from other sites; Lead or support transfer projects, ensuring they are completed within set timelines; Facilitate proper transfer of tests to QC laboratories for commercial batch release; Participate in or lead transfer-related activities, including development, implementation, and post-transfer testing; Act as the primary contact for deviations, changes, audits, training, and documentation, ensuring compliance with GMP procedures; Use Lean Six Sigma tools for problem-solving, process improvements, and continuous quality enhancement. Requirements: HBO level education in (micro)biology, analytical chemistry, or similar field; Minimum of 5 years’ experience in a biological QC laboratory, preferably within GMP or GLP environments; Proven expertise in transfer processes, data analysis, and root cause investigation; Experience with change management and project leadership is advantageous; Familiarity with SAP, LIMS, and electronic QC data systems; Certified Yellow Belt or experienced with Lean/Six Sigma methodologies is a plus; Accurate, proactive, and solution-oriented with strong communication skills in English and Dutch.
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