Senior Operator Packaging 2 pl.

• Operations & Maintenance
• Netherlands, Amsterdam
• June 5, 2026
• Fulltime
• mbo-4, mbo, hbo
• V-179215-1
• €0 - €5316.05 per month

About the Role

As a Senior Operator Packaging, you will perform pharmaceutical packaging activities for blood plasma and related (intermediate) products under strict GMP guidelines. You will lead operational activities, contribute to process improvements, supervise team members, and ensure the highest levels of quality and compliance. This role is essential in maintaining safe, efficient, and compliant production processes within a highly regulated environment.

Key Responsibilities

1. Managing Part of the Production Process

1. Maintain up-to-date knowledge of relevant production stages.
2. Manage control methods and equipment within own production area.
3. Advise supervisors on process improvements and modifications.
4. Troubleshoot production issues and coordinate with internal/external stakeholders.
5. Lead improvement projects after approval.
6. Complete required production-related administration and communication.
7. Deliverable: A well-functioning production process supported by current knowledge and optimized workflows.

2. Performing Production Operations

1. Execute production activities according to SOPs and GMP regulations.
2. Perform calculations (e.g., dilutions).
3. Prepare materials and clean equipment after production.
4. Record all activities in logbooks and batch documentation.
5. Identify and report deviations to the supervisor.
6. Register raw/auxiliary materials and rejected materials in the system.
7. Perform minor technical maintenance and support technicians when needed.
8. Maintain stock levels and ensure timely replenishment.

3. Training Employees & Ensuring Quality Compliance

1. Train and requalify employees.
2. Introduce new or updated GMP regulations and ensure proper implementation.
3. Ensure correct and consistent documentation (logbooks, batch records).
4. Oversee protocol compliance and proper deviation documentation.
5. Manage routine qualification planning.
6. Result: A trained and competent team working fully in line with GMP procedures.

4. Monitoring Quality & Quality Systems

1. Write validation, calibration, and quality protocols.
2. Perform quality checks and sampling for materials, processes, and products.
3. Deliver samples to testing areas and record results.
4. Implement corrective changes following audit findings.
5. Monitor WFI systems and cleanroom/work areas.
6. Resolve internal complaints and coordinate Alertboard items.
7. Support new process implementation in coordination with QA.
8. Outcome: Controlled, compliant processes with continuous quality improvement.

5. Operational Team Leadership

1. Plan and coordinate daily work for the team.
2. Lead work meetings, coach team members, and maintain team motivation.
3. Assess work quality and address issues when needed.
4. Provide performance-related input to the Supervisor.
5. Deliverable: A motivated team delivering high-quality work on schedule.

Your Profile

1. Bachelor’s degree in a relevant field OR equivalent experience.
2. 5+ years of experience in a GMP-controlled production environment.
3. Strong experience in pharmaceutical packaging processes.
4. Detail-oriented, structured, proactive, and a team player.
5. Fluent in Dutch and English.
6. Willing to work in 2 shifts.

What We Offer

1. Full-time position (40h) with a competitive salary.
2. 14.83% shift allowance.
3. 8.33% end-of-year bonus & 8.33% holiday allowance.
4. €2,100 personal training budget every 3 years.
5. Travel allowance from the first kilometer.
6. Good accessibility by public transport + private parking.
7. Pension scheme via Zorg & Welzijn.
8. A dynamic, safe, and innovative working environment with opportunities for professional growth—while contributing to the health of millions.