MedTech Production Operator — Groningen (Full-time)

Johnson & Johnson Innovative Medicine; Groningen; On-site; EUR 34,000 - 51,000; Full time

Job summary

Johnson & Johnson seeks a skilled Production Operator for its Groningen facility to join a sterile, controlled AMO environment and contribute to high-quality lens production. The role requires 5+ years in a production setting, precise visual/microscopic inspection, and data recording to support safety and quality.

The successful candidate will work full-time shift work, comply with GMP and hygiene standards, and participate in training on international quality rules.

Qualifications

• Minimaal MBO‑3 diploma of aantoonbaar gelijkwaardig werkniveau.

Responsibilities

• Uitvoeren van productiehandelingen in meerdere procesfasen (draaien, frezen, oppervlaktebehandeling, inspectie) om hoogwaardige producten te leveren.
• Monitoren en bijsturen van machines en procesparameters om productkwaliteit en -veiligheid te waarborgen.
• Uitvoeren van visuele en microscopische controles en nauwkeurig vastleggen van product‑ en procesdata.
• Werken volgens GMP‑, hygiëne‑ en veiligheidsvoorschriften om een schone en gecontroleerde productieomgeving te behouden.
• Samenwerken met het team om procesproblemen op te lossen en verbeteringen door te voeren die de betrouwbaarheid verhogen.
• Naleven van procedures en bijdragen aan een consistente, foutarme productiestroom.

Skills

Administrative Support

Agile Manufacturing

Assembly Operations

Detail-Oriented

Execution Focus

Factory Acceptance

GMP

Innovation

Learning Agility

Manufacturing Processes

MSAT

Mechanical Equipment

Plant Operations

Process Oriented

Prototyping

Repair Management

Structural Fabrication

Technologically Savvy

Education

MBO-3 diploma

Tools

SAP

Job description

Johnson & Johnson seeks a skilled Production Operator for its Groningen facility to join a sterile, controlled AMO environment and contribute to high-quality lens production. The role requires 5+ years in a production setting, precise visual/microscopic inspection, and data recording to support safety and quality.

The successful candidate will work full-time shift work, comply with GMP and hygiene standards, and participate in training on international quality rules.