Manufacturing Operator

Sire Search; Haarlem; Sur place; EUR 28 000 - 38 000; Plein temps

Résumé du poste

Sire Search is seeking Production Operators to support pharmaceutical manufacturing in a regulated GMP environment. You will gain hands-on experience with production processes, equipment operation, and quality systems.

Fluent Dutch and English, you will follow SOPs, maintain safety and quality, and contribute to a clean, compliant production area while collaborating with a dedicated team. This role involves rotating shifts and structured training to build a solid GMP foundation.

Qualifications

• MBO level education in a technical, manufacturing, engineering, pharmaceutical, biotechnology, or life sciences discipline.
• Fluent Dutch and English, written and verbal.
• Ability to work in a structured and regulated manufacturing environment.
• Strong attention to detail and commitment to quality.
• Understanding of GMP principles is advantageous.
• Willingness to work in rotating shift patterns.

Responsabilités

• Execute production activities according to approved procedures, GMP requirements, and safety standards.
• Prepare production materials, equipment, and work areas for operational activities.
• Operate production equipment following training and approved instructions.
• Complete accurate and timely documentation of all assigned activities.
• Follow GMP guidelines and quality requirements at all times.
• Identify deviations, abnormalities, and safety concerns and elevate appropriately.
• Support smooth shift handovers and maintain effective communication within the team.
• Participate in training programs and on the job learning activities.
• Contribute to maintaining a safe, clean, and compliant production environment.
• Collaborate with operators and production colleagues to ensure operational continuity.

Connaissances

Dutch language

English language

GMP knowledge

Attention to detail

Team player

Structured approach

Formation

MBO level education

Description du poste

The Company

A global pharmaceutical manufacturing organization focused on producing high quality medicines and healthcare products. The company operates in highly regulated production environments with a strong emphasis on safety, operational excellence, quality compliance, and continuous employee development

About the Role

We are seeking motivated Production Operators to support manufacturing activities in a regulated pharmaceutical production environment. This position is ideal for candidates looking to build a strong foundation in GMP manufacturing while gaining hands on experience with production processes, equipment operation, and quality systems.

Responsibilities

• Execute production activities according to approved procedures, GMP requirements, and safety standards
• Prepare production materials, equipment, and work areas for operational activities
• Operate production equipment following training and approved instructions
• Complete accurate and timely documentation of all assigned activities
• Follow GMP guidelines and quality requirements at all times
• Identify deviations, abnormalities, and safety concerns and elevate appropriately
• Support smooth shift handovers and maintain effective communication within the team
• Participate in training programs and on the job learning activities
• Contribute to maintaining a safe, clean, and compliant production environment
• Collaborate with operators and production colleagues to ensure operational continuity

Requirements

• MBO level education, preferably in a technical, manufacturing, engineering, pharmaceutical, biotechnology, or life sciences discipline
• Fluent Dutch and English language skills, both written and verbal
• Ability to work in a structured and regulated manufacturing environment
• Strong attention to detail and commitment to quality
• Understanding of GMP principles is advantageous
• Willingness to work in rotating shift patterns
• Strong team player with good communication skills
• Reliable, accurate, and safety conscious work approach
• Ability to learn new processes and technologies quickly
• Flexible and adaptable mindset
• Comfortable following standard operating procedures
• Eligible to complete PESV screening