Production Coordinator
Content + Source + Freshness • 12 Dec 2025 • 95% confidence
Offer value
High value positioned in the medical device assembly industry with career advancement potential, but demands strong regulatory knowledge.
- Role critical for quality assurance in medical devices
- Growth opportunities in a high-demand sector
- Requires strong understanding of industry regulations
Pros
- Significant impact on product quality in a medical environment
- Non-corporate culture with strong career growth opportunities
- Clear role responsibilities and promotion paths
Cons
- Requires in-depth knowledge of regulatory standards
- May experience high pressures to meet production deadlines
- Role demanding attention to detail under possible time constraints
Who it's for
Mid-level • On-site in Delft, Netherlands
Good fit
- Mid-level quality engineers or production coordinators
- Candidates with medical device manufacturing experience
- Individuals keen on contributing to health tech advancements
Not recommended for
- Entry-level candidates without manufacturing experience
- Those favoring less pressure in work settings
- Individuals uninterested in compliance and regulatory matters
Motivation fit
Key skills
About the job
Job Summary:
We are seeking a highly skilled and experienced Engineer to join our medical device assembly team. The Production Coordinator will be responsible for ensuring that we are operating at maximum efficiency and that our medical devices are manufactured to the highest quality standards.
Key Responsibilities:
- Production Planning and Scheduling
- Production Team Training
- Production Quality Assurance
- Conduct quality checks and inspections to verify that products meet quality standards
- Develop, implement and maintain quality systems and procedures for medical device assembly
- Provide guidance and support to production staff to ensure compliance with quality standards
- Develop and implement quality control plans and procedures for incoming materials, in-process materials, and finished products
- Analyze quality data and metrics to identify trends and areas for improvement
- Participate in root cause analysis investigations of quality issues and develop corrective actions to prevent reoccurrence
- Work with cross-functional teams to develop and implement process improvements
- Ensure compliance with regulatory requirements and company policies
- Facility and Environment Management (cleanliness)
Qualifications and Skills:
- Bachelor's degree in mechanical engineering
- Minimum of 2-3 years of experience in quality engineering or quality control in a manufacturing environment
- Strong knowledge of quality systems and regulations in the medical device industry (FDA, ISO, etc.)
- Experience with process validation, including IQ/OQ/PQ
- Strong analytical and problem-solving skills
- Excellent written and verbal communication skills
- Ability to work in a team environment and lead cross-functional teams
- Strong project management skills
- Ability to prioritize and manage multiple tasks and projects simultaneously
If you are a highly skilled and experienced engineer with a strong background in medical device assembly, we encourage you to apply. We offer a competitive salary, comprehensive benefits, and opportunities for career growth and development.
