Production Operator

SIRE LIFE SCIENCES; Breda; On-site; EUR 30,000 - 40,000; Full time

Job summary

A global pharmaceutical organization located in Breda, Netherlands, seeks a Production Operator to ensure the efficient operation of production lines. The ideal candidate has 1–2 years of manufacturing experience, familiarity with GMP principles, and a pro-active approach to continuous improvement. Responsibilities include operating production lines, collaborating with team members, and maintaining compliance with safety and quality standards. This role offers a flexible shift pattern and emphasizes teamwork and accountability.

Qualifications

• 1–2 years of experience in a manufacturing environment, preferably within pharmaceuticals.
• Familiarity with Standard Operating Procedures and GMP principles.
• Ability to work effectively in a multi‑cultural team.

Responsibilities

• Operate production lines according to standard operating procedures.
• Collaborate with team members to achieve daily performance targets.
• Participate actively in shift handovers.

Skills

Manufacturing experience

GMP principles

Effective communication

Flexibility

Proactive attitude

Education

General MBO (Level 2) education or equivalent

Job description

About the Company

A global pharmaceutical and medical device organisation recognised for its commitment to quality, compliance, and innovation. The company operates under strict GMP regulations and supports advanced manufacturing and validation processes.

About the Role

This position involves operating and maintaining production lines within a pharmaceutical environment, ensuring adherence to GMP standards and safety protocols. The role requires flexibility to work across multiple lines and shift patterns, while maintaining efficiency, accuracy, and a proactive approach to continuous improvement.

Responsibilities

• Operate production lines according to standard operating procedures.
• Collaborate with team members and line leads to achieve daily performance targets.
• Escalate issues promptly and accurately when necessary.
• Participate actively in shift handovers and maintain clear communication.
• Ensure all required training is completed within deadlines.
• Identify opportunities for process improvement and efficiency.
• Maintain compliance with safety, quality, and inventory standards.

Requirements

• 1–2 years of experience in a manufacturing environment (preferably pharmaceutical, GMP/GDP).
• Familiarity with Standard Operating Procedures and GMP principles.
• Ability to work in a multi‑cultural team and communicate effectively in English.
• General MBO (Level 2) education or equivalent.
• Flexible and adaptable to different tasks and shift patterns.
• Strong sense of accountability and responsibility.
• Structured, disciplined, and accurate in work execution.
• Proactive attitude and willingness to learn continuously.

Other Information

• Shift pattern: 2 or 3 shift(s), 5‑day schedule.
• Work across fully automated, semi‑automated, and manual production lines.
• Requires strong focus on safety, quality, and performance metrics.