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Manufacturing Operator
Job in
2000, Haarlem, North Holland, Netherlands
Listed on 2026-10-19
Listing for:
Sire Search
Full Time
position Listed on 2026-10-19
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Production Associate / Production Line, Manufacturing & Industrial Operations, Production QC/QA
Job Description & How to Apply Below
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 RoleWe 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
- 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
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