Production Operator

Production Operator (GMP) for a pharmaceutical site in Haarlem, temporary full-time contract (1 year), on-site shift work.

Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)

Eisen

  • Fluent in both Dutch and English (spoken and written)
  • Accurate, detail-oriented working style and strong discipline in following procedures
  • Willing/able to work 16/5 or 24/5 shifts (incl. nights)
  • Team-oriented attitude with clear communication during handovers and daily collaboration
  • Comfortable working in a structured, regulated production environment

Wensen

  • MBO level education, preferably in a technical, production, or life-science related field
Volledige omschrijving

Company: Our client is a leading organisation within the pharmaceutical manufacturing sector, operating a highly regulated production site in the Netherlands. The company is known for strong quality standards, structured ways of working, and a strong focus on safety, compliance, and continuous learning on the shopfloor.

Job Description: For a regulated production site in Haarlem, we are looking for a Production Operator (GMP Environment). In this role, the operator supports daily production by executing assigned tasks safely, accurately, and fully in line with approved procedures. The position suits someone who enjoys structured work, takes ownership of doing things right the first time, and escalates issues quickly when something deviates from the standard.

Responsibilities: The Production Operator (GMP Environment) will execute assigned production activities according to approved procedures, safety requirements, and quality standards; prepare tasks, materials, and work areas as instructed; operate equipment as trained and follow agreed working methods; apply GMP principles and ensure correct, timely documentation of all own activities; recognise deviations, abnormalities, or safety concerns and escalate them in line with established escalation rules; work closely with colleagues within the production team and follow structured handover and communication practices; and participate in training and on-the-job learning to build technical knowledge and practical skills.

Requirements: MBO level education, preferably in a technical, production, or life-science related field; fluent in both Dutch and English (spoken and written); comfortable working in a structured, regulated production environment; accurate, detail-oriented working style and strong discipline in following procedures; team-oriented attitude with clear communication during handovers and daily collaboration; temporary full-time contract (1 year); willing/able to work 16/5 or 24/5 shifts (incl. nights).

Other Information: This role is based on-site in Haarlem and involves working in a structured shift environment. A pre-employment screening may be part of the process.

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