Open for applications

Senior Manufacturing Operator

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About the vacancy

Engineering
Process Automation
Manufacturing Engineering
Process Engineering
General
Manufacturing
Quality
Quality Control
Compliance
Regulatory Affairs
Regulatory compliance
Expert Vocational Training (MBO) Permanent Full time 38,300.00 to 61,410.00 Leiden, South Holland, Netherlands

About Your Next Job

We are searching for the best talent for Senior Manufacturing Operator to be based in Leiden.

We are looking for a hands‑on Manufacturing Process Specialist who will support Operations by executing day‑to‑day manufacturing tasks, maintaining high quality and regulatory standards, and helping the team meet production targets. You will work closely with colleagues to keep processes running smoothly, respond to interruptions, and contribute to continuous improvement.




About Your Tasks and Responsibilities

As a Manufacturing Process Specialist, you will:

  • Implement routine manufacturing tasks accurately and on time to meet production targets and maintain operational flow.
  • Follow and promote GMP, SOPs, and company policies, ensuring tasks meet regulatory and internal quality standards.
  • Supervise in‑process parameters, raise deviations or non‑conformances, and take immediate corrective steps to reduce disruption.
  • Coordinate daily planning, prioritisation, and handovers to support smooth operations and clear team communication.
  • Keep clear, timely records and complete required training to ensure traceability and reliable documentation.
  • Identify and record process improvements, collaborate on solutions, and drive sustainable changes that improve safety, quality, and efficiency.


About Your Skills and Experience

Qualifications/Requirements:

  • Relevant MBO‑3 degree in a technical field with at least 3 years’ proven experience, or a non‑relevant MBO‑3 degree with at least 5 years’ proven experience.
  • Good in coordination and communication.
  • Experience in problem solving and planning.
  • Working proficiency in Dutch and English at approx. B1 level.
  • Practical knowledge of GMP and regulatory issues, able to apply standards in daily tasks and support audits/CAPAs.
  • Computer skills: intermediate MS Office, entry‑level data analysis, and specialist level in business applications.
  • Reliable, proactive, and stress‑resilient: able to work independently, as part of a team, and adapt to new ways of working.
  • Willingness and ability to work on a shift roster and follow administrative processes to ensure accurate, timely deliverables.



You are eligible to work in EU

We only accept applicants who are eligible to work in the EU


Contact person

logo of Johnson & Johnson

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com



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