Validation & Calibration Specialist
GMP Validation & Calibration Specialist voor een farmaceutische opdrachtgever, on-site in Boxmeer, via SIRE Life Sciences.
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Eisen
- Fluent Dutch
- HBO-level education (or equivalent)
- Hands-on experience with validation, calibration, and technical documentation/reporting
- Proven experience in a GMP/pharmaceutical environment
- Able to work accurately and independently, productive quickly in an autonomous role
- Strong English skills (spoken and written)
Wensen
- Experience with autoclaves, temperature measurements, and process equipment
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Company: Our client is a large, highly regulated organization within the pharmaceutical sector, operating a modern production site where quality, compliance, and safety are critical. The site works under GMP standards and relies on robust processes, clear documentation, and well-maintained equipment to ensure reliable operations.
Job Description: For an on-site role in Boxmeer (Netherlands), we are looking for a GMP Validation & Calibration Specialist who can independently support validation and calibration activities in a GMP environment. The GMP Validation & Calibration Specialist combines hands-on technical work with strong documentation skills, ensuring all work is executed in line with SOPs and work instructions and recorded accurately in both Dutch and English.
Responsibilities: Perform validation and calibration activities on-site within a GMP pharmaceutical environment. Work strictly according to SOPs and work instructions, ensuring consistent compliance. Prepare, maintain, and deliver clear technical documentation, reports, and records with a high level of accuracy. Support reliable and compliant operations by recording results precisely and following good documentation practices. Support activities involving temperature measurements and process equipment; autoclave-related knowledge is relevant to the work.
Communicate effectively in both Dutch and English, including working with Dutch-language procedures and documentation.
Requirements: Completed HBO-level education (or equivalent). Proven experience in a GMP/pharmaceutical environment. Hands-on experience with validation, calibration, and technical documentation/reporting. Fluent Dutch (required) and strong English skills (spoken and written). Able to work accurately and independently, with enough experience to be productive quickly in an autonomous role. Nice to have experience with autoclaves, temperature measurements, and process equipment.
Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.
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