Assembly Manufacturing Supervisor — Lean, GMP, Lead Teams

Brighter Signals

Leiden

On-site

EUR 54,000 - 85,000

Full time

6 days ago
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Benefits offered by this job

Annual bonus
Vacation days
Parental leave (min 12 weeks)
Bereavement leave
Well-being reimbursement

Job summary

Johnson & Johnson in Leiden, Netherlands, is seeking a Manufacturing Supervisor to lead end‑to‑end production operations, ensuring high‑quality products are made safely and in full cGMP compliance. You will work with cross‑functional teams to meet the Master Production Schedule while promoting continuous improvement.

The role requires a minimum 5 years of manufacturing experience, a HBO‑level degree, and strong English/Dutch communication.

Qualifications

  • Bachelor’s degree (HBO level) with at least 5 years of manufacturing experience.
  • Experience in medical device or regulated manufacturing industry.
  • Knowledge of cGMP, EHS and quality systems in production.

Responsibilities

  • Lead and supervise manufacturing teams to achieve production targets in line with the Master Production Schedule.
  • Assign operators, manage resource needs, and ensure adequate assets and staffing levels.
  • Support the introduction, qualification, and validation of new products and equipment, including training of operators.
  • Ensure all process documentation, SOPs, and work instructions are accurate, current, and completed on time.
  • Monitor manufacturing performance through data analysis and implement corrective actions.
  • Lead or support deviation investigations, CAPAs, and change management activities.
  • Drive continuous improvement initiatives and act as a subject matter expert for assigned processes.

Skills

Leadership
Coaching
Data analytics
Lean Six Sigma
English & Dutch

Education

Bachelor’s degree (HBO level)

Tools

ERP
Excel
Windows-based tools

Job description

Johnson & Johnson in Leiden, Netherlands, is seeking a Manufacturing Supervisor to lead end‑to‑end production operations, ensuring high‑quality products are made safely and in full cGMP compliance. You will work with cross‑functional teams to meet the Master Production Schedule while promoting continuous improvement.

The role requires a minimum 5 years of manufacturing experience, a HBO‑level degree, and strong English/Dutch communication.

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