Automated Production Systems Technician
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Automated Production Systems Technician in Breda, Noord-Brabant, pharmaceuticals sector, start 31 juli 2026.
- Locatie
- Breda
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- Windimi Post
Eisen
- Capable of documenting activities following GMP standards
- Fluency in English
- Ability to participate in triage and problem-solving sessions
- Minimum 3 years' experience in a similar production or manufacturing role
- Willingness to work in shifts and commute as required
- Proven experience working with automated production systems
- Comfortable working in a structured environment with strict procedures
Omschrijving
A leading global biotechnology organization, dedicated to developing and delivering innovative medicines to improve patient outcomes, is seeking a skilled Automated Production Systems Technician to support the operation and optimization of advanced, automated manufacturing lines. The role involves ensuring production runs smoothly, adhering to GMP standards, and contributing to process improvements within a regulated environment. Responsibilities include operating and overseeing automated production equipment following SOPs and GMP requirements, troubleshooting issues and conducting root cause analysis, adjusting mechanical and process parameters to maximize machine performance, recording and managing production data in SAP/MES systems, monitoring process performance and identifying deviations, preparing accurate GMP documentation including batch records and logs, participating in problem solving sessions with QA, Engineering, and Production teams, and carrying out equipment setup and shutdown procedures. Requirements include a minimum of 3 years' experience in a similar production or manufacturing role, ideally in assembly and packaging, proven experience with automated production systems, fluency in English, comfort in a structured environment with strict procedures, willingness to work in shifts and commute as required, ability to participate in triage and problem-solving sessions, and capability to document activities following GMP standards. The position is located in Breda, Noord-Brabant, in the pharmaceuticals sector, with a start date of 31 July 2026.
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