Production Operator Manual Lines Blue

Real; Breda; On-site; EUR 31,000 - 42,000; Full time

Job summary

Real seeks a Production Operator on manual lines in Breda to assemble, label, inspect, and package medicines for patients worldwide. The role operates in a GMP-regulated environment, emphasizing quality, safety, and precise documentation within a mainly manual, repetitive workflow.

Initially 2 shifts, the position will move to 5 shifts from January 2027. Candidates should have 2 years in production, be willing to commute to Breda, and work under SOPs and quality standards; pharmaceutical

Qualifications

• At least 2 years of experience in a production environment.
• Experience with manual production, assembly, or packaging activities.
• Strong attention to detail and product quality.
• Willing to commute to Breda and start in a 2-shift system; move to 5 shifts from January 2027.

Responsibilities

• Perform manual production, assembly, labelling, and packaging activities
• Follow SOPs, work instructions, and GMP requirements
• Inspect products and perform production quality checks
• Complete batch records, production logs, and other documentation accurately
• Identify and report production deviations
• Support the investigation and resolution of production issues
• Participate in problem-solving meetings between Quality and Production
• Perform line set-up and close-down activities
• Carry out cleaning activities according to established procedures
• Maintain a consistent work pace without compromising quality
• Ensure a safe, clean, and structured working environment
• Communicate clearly with colleagues during the shift

Job description

Schedule: Initially 2 shifts, moving to 5 shifts from January 2027

Industry: Pharmaceutical manufacturing

Role Overview

As a Production Operator on manual lines, you help ensure that medicines are correctly assembled, labelled, inspected, and packaged before being shipped to patients worldwide.

You work in a structured, GMP-regulated production environment where quality, safety, and accurate documentation are essential. The work is mainly manual and repetitive, so you must be able to stay focused, work accurately, and maintain a consistent production pace throughout your shift.

Key Responsibilities

• Perform manual production, assembly, labelling, and packaging activities
• Follow SOPs, work instructions, and GMP requirements
• Inspect products and perform production quality checks
• Complete batch records, production logs, and other documentation accurately
• Identify and report production deviations
• Support the investigation and resolution of production issues
• Participate in problem-solving meetings between Quality and Production
• Perform line set-up and close-down activities
• Carry out cleaning activities according to established procedures
• Maintain a consistent work pace without compromising quality
• Ensure a safe, clean, and structured working environment
• Communicate clearly with colleagues during the shift

Basic Requirements

• At least 2 years of experience in a production environment
• Experience with manual production, assembly, or packaging activities
• Strong attention to detail and product quality
• Able to perform repetitive manual tasks accurately and consistently
• Comfortable working according to strict procedures and work instructions
• Reliable, disciplined, and team-oriented
• Willing to commute to Breda
• Willing to start in a 2-shift system
• Willing to move to a 5-shift system from January 2027

Experience in pharmaceutical manufacturing is preferred, but candidates from other structured production environments, such as food, medical devices, cosmetics, or packaging, are also encouraged to apply.

Core Competencies

• Accuracy and attention to detail
• Strong quality and safety awareness
• Consistent and structured way of working
• Ability to maintain focus during repetitive tasks
• Reliability and personal responsibility
• Ability to follow procedures and work instructions
• Effective communication and teamwork
• Willingness to learn and develop

GMP and Operational Experience

Experience with the following is an advantage:

• GMP-regulated production
• Standard Operating Procedures
• Production or quality documentation
• Batch records and production logs
• Manual quality inspections
• Set-up and close-down activities
• Cleaning procedures
• Pharmaceutical, food, medical-device, or other regulated production