Operator A - GMP Production Role in Pharmaceutical Industry

Further Details

We are seeking a dedicated Operator A to join our pharmaceutical production team, operating within a stringent GMP framework. This role is pivotal for maintaining the high standards of our manufacturing processes, focusing on precision, efficiency, and collaboration. You will be instrumental in operating, configuring, and maintaining critical production machinery, gaining comprehensive understanding of the entire product lifecycle and contributing to process enhancements. This is a fantastic opportunity for individuals with a strong technical aptitude and a commitment to quality. This is an essential role for a technically proficient individual who thrives in a regulated production setting. As an Operator A, you will be directly involved in the day-to-day operations, including machine setup, minor troubleshooting, and quality documentation. Your contribution will extend to identifying production deviations and participating in improvement projects, fostering a proactive approach to manufacturing excellence. We prioritize continuous learning and offer extensive avenues for both personal and professional growth.

Operator A - Pharmaceutical Production Opportunities

JR Netherlands is actively recruiting for an Operator A position within a leading pharmaceutical company operating under strict Good Manufacturing Practice (GMP) standards. This role is crucial for ensuring the smooth and efficient functioning of production lines, demanding a high level of technical proficiency and a commitment to quality.

The ideal candidate will possess a minimum of three years' experience in regulated industries such as pharmaceuticals, food, or high-tech manufacturing, holding at least an MBO level 3 qualification. You will be responsible for machine operation, setup, maintenance, and contributing to process optimization, making this a dynamic and engaging career opportunity for those seeking professional growth in a highly respected sector. Competitive salary and benefits are offered.

• Job Title: Operator A
• Industry: Pharmaceutical Manufacturing
• Location: Oud-Beijerland, Zuid-Holland, Netherlands
• Experience Required: 3+ years in pharma, food, or high-tech
• Education: MBO level 3 or equivalent
• Key Responsibilities: Machine operation, GMP compliance, quality documentation, process improvement
• Salary Range: €2,664.75 - €3,473.99 gross per month (full-time)
• Benefits: 25 vacation days, 13 ATV days, premium-free pension, travel allowance, lease bike plan

Skills

• Minimum 3 years of experience in pharmaceutical, food, or high-tech industries
• Technical insight for machine setup and troubleshooting
• Ability to work within GMP guidelines
• Strong understanding of production processes
• Capability to train and guide new employees
• Good physical condition

Duties and Responsibilities:

• Setting up and operating machines according to GMP guidelines
• Performing maintenance and resolving minor technical issues
• Contributing to the update of work processes
• Completing and reviewing batch documentation accurately
• Identifying and reporting production deviations
• Participating in improvement projects
• Training and mentoring new staff members
• Operating machinery in the Preparation, Filling, or Packaging departments

How to apply

• Application Process: Prospective candidates are encouraged to apply for the Operator A role via the Eurojobs platform.
• Required Documents: A comprehensive CV detailing relevant experience and qualifications is essential.
• Eligibility: Applicants must have a minimum of three years' experience in the pharmaceutical, food, or high-tech manufacturing sectors and hold at least an MBO level 3 qualification.
• Availability: Candidates must be available to work flexible hours between 06:00 and 20:00.
• Application Link: Click on the 'Apply Now' button on the Eurojobs website to submit your application.
• Job Reference: Ensure you note the job reference number: 7fc606fefe79bd15e48d8897a4c6365a.
• Deadline: All applications must be submitted by December 18, 2026.
• Further Development: Opportunity to obtain the 'Farmaceutisch Vakman' certificate.