Lead MedTech Operator - Production

Eurofins Scientific - Nederland; Nijmegen; On-site; EUR 55,000 - 75,000; Full time

Benefits offered by this job

31 vacation days per year

Specialist training

Flexible start times

Mental health platform access

Bike purchase program

Job summary

Eurofins Scientific Nederland in Nijmegen seeks a Lead MedTech Operator - Production to combine hands-on manufacturing with team leadership in a regulated MedTech environment.

You will perform production activities under GxP guidelines, coordinate daily operations, and work closely with the Site Lead and the client’s Production Manager to ensure smooth operations and continued product quality.

Qualifications

• Experience leading teams in a regulated production environment.
• Strong communication with operators, management and stakeholders.
• Proven ability to coach colleagues and drive quality and continuous improvement.

Responsibilities

• Manufacture the product per procedures and quality standards.
• Prepare and verify batch components and related documentation.
• Lead one-on-one meetings to support team development and engagement.
• Coordinate production planning and allocate resources effectively.
• Act as primary operational contact for the client's Production Manager.
• Support onboarding and training of new operators.
• Lead by example with professionalism and accountability.

Skills

Leadership

Coaching

Communication

Team collaboration

Quality focus

Education

MLO/HBO Life Sciences

Job description

For our team in Nijmegen, we are looking for a Lead MedTech Operator - Production who combines hands-on production work with team leadership responsibilities in a regulated MedTech environment. In this role, you will support the manufacturing of an innovative product used by patients worldwide while helping to coordinate daily operations and support the development of the production team.

As a Lead MedTech Operator, you will spend a significant part of your time performing production activities according to GxP guidelines and established procedures. In addition, you will act as a key point of contact within the team, support production planning, and work closely with both the Site Lead and the client\'s Production Manager to ensure smooth and efficient operations.

Tasks and Responsibilities

• Manufacturing the product according to procedures, Good Manufacturing and Documentation Practices and the quality standards of the area.
• Preparing and completing documentation for the various manufacturing steps.
• Preparing and verifying batch components.
• Inspecting product quality according to specifications.
• Cleaning the work area to avoid contamination and/or mixing of products.
• Conducting regular one-on-one meetings with team members to support their development and engagement.
• Supporting the Site Lead by providing insight into team performance, challenges, and improvement opportunities.
• Assisting with production planning and helping to ensure resources are effectively allocated.
• Acting as the primary operational contact for the client\'s Production Manager.
• Supporting the onboarding and training of new operators.
• Leading by example through professionalism, accountability, and a strong commitment to quality.

Qualifications

• You have an MLO or HBO degree, preferably in Life Sciences, Biotechnology, Chemistry, or a related field.
• You have 3-5 years of experience in a production environment, preferably within MedTech, pharmaceutical, biotechnology, or another regulated industry.
• You have demonstrated leadership skills and enjoy coaching and supporting colleagues.
• You communicate effectively with operators, management, and client stakeholders.
• You are organized, proactive, and able to maintain oversight in a dynamic production environment.
• You have a strong focus on quality, compliance, and continuous improvement.
• You are fluent in English, both spoken and written.

What working at PSS means

Working at PSS means working in a team where people support each other, take responsibility for their work and stay closely connected to the client environment they work in. You will be part of an international setting, with colleagues who value clear communication, teamwork and a good working atmosphere.

We believe it is important that people can keep developing in their role. That is why we offer specialist training and opportunities to build your knowledge and skills further. We also make time to stay connected as a team, for example through monthly team lunches, team activities and moments where colleagues are recognized for their contribution.

We offer

• A responsible position within the team;
• Room to share your ideas and input;
• Specialist training and opportunities for personal and professional development;
• 31 vacation days per year based on a full-time employment contract, with the option to purchase 5 additional days;
• The option to use gross/net benefit schemes for sports and the purchase of a bicycle;
• Access to an online preventive mental health platform;
• A flexible start time between 07:00 and 09:00, depending on team planning and operational needs;

Working at PSS gives you the personal approach of a medium-sized organization, with the wider network and structure of Eurofins as a parent company. In your work, you regularly interact with other companies and scientists within the Eurofins group, which brings variety to the role.

This also means there may be opportunities to grow, depending on your role, experience and development.