Production Manager Assistant

Qabird; Pijnacker; On-site; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Career growth opportunities

Job summary

Qabird is seeking an experienced Engineer to join their medical device assembly team in Pijnacker, Netherlands. The Production Coordinator will ensure the highest quality standards and operational efficiency in manufacturing.

Key responsibilities include production planning, quality assurance, and training production staff. Qualifications required are a Bachelor's degree in mechanical engineering and 2-3 years of relevant experience. A competitive salary and comprehensive benefits are offered.

Qualifications

• 2-3 years of experience in quality engineering or quality control in manufacturing.
• Strong knowledge of FDA and ISO regulations in the medical device industry.
• Experience with process validation (IQ/OQ/PQ).

Responsibilities

• Plan and schedule production activities.
• Train production team on quality assurance practices.
• Conduct quality checks and maintain quality systems.

Skills

Quality systems knowledge

Analytical skills

Problem-solving skills

Teamwork

Project management

Communication skills

Education

Bachelor's degree in mechanical engineering

Job description

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

1. Production Planning and Scheduling
2. Production Team Training
3. Production Quality Assurance
   1. Conduct quality checks and inspections to verify that products meet quality standards
   2. Develop, implement and maintain quality systems and procedures for medical device assembly
   3. Provide guidance and support to production staff to ensure compliance with quality standards
   4. Develop and implement quality control plans and procedures for incoming materials, in-process materials, and finished products
   5. Analyze quality data and metrics to identify trends and areas for improvement
   6. Participate in root cause analysis investigations of quality issues and develop corrective actions to prevent reoccurrence
   7. Work with cross-functional teams to develop and implement process improvements
   8. Ensure compliance with regulatory requirements and company policies
4. Facility and Environment Management (cleanliness)

Qualifications and Skills

1. Bachelor's degree in mechanical engineering
2. Minimum of 2-3 years of experience in quality engineering or quality control in a manufacturing environment
3. Strong knowledge of quality systems and regulations in the medical device industry (FDA, ISO, etc.)
4. Experience with process validation, including IQ/OQ/PQ
5. Strong analytical and problem-solving skills
6. Excellent written and verbal communication skills
7. Ability to work in a team environment and lead cross-functional teams
8. Strong project management skills
9. 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.