QC Supervisor - Medical Devices (GMP/ISO 13485)

Sinclair; Almere; On-site; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Competitive Salary

Career Growth & Learning Opportunities

13th month bonus

25 vacation days

8% holiday pay

Travel allowance based on €0,23/km

Retirement savings plan

Job summary

Sinclair is hiring a Supervisor Quality Control at our Almere facility in the Netherlands. You will lead the QC Analysts, plan daily/weekly activities, and ensure timely testing across chemical, physical, and microbiological methods in a Class III medical device environment.

The role requires a HLO/Bachelor's degree, strong leadership, and fluency in English and Dutch, with 3+ years of supervisory experience in regulated labs. On-site position with GMP/ISO13485 adherence.

Qualifications

• Bachelor's degree in Laboratory Techniques or related field (or equivalent).
• Fluent in English; Dutch proficiency preferred.
• Minimum 3 years of team leadership in a regulated lab/QC setting.

Responsibilities

• Supervise, coach, and support QC Analysts in daily operations.
• Create and manage daily/weekly QC team planning to meet test turnaround times.
• Train new QC Analysts and maintain competency matrix.
• Act as backup for Quality Manager during absences.
• Conduct performance conversations and contribute to appraisals.
• Oversee chemical, physical, and microbiological QC testing per approved methods.
• Ensure QC testing meets timelines for batch disposition.
• Review and release incoming raw materials in ERP/QMS.
• Review batch record test data for completeness and accuracy.

Skills

Team leadership

QC testing

Planning

Excel & ERP

Education

Bachelor's degree

Tools

ERP/QMS systems

Job description

Sinclair is hiring a Supervisor Quality Control at our Almere facility in the Netherlands. You will lead the QC Analysts, plan daily/weekly activities, and ensure timely testing across chemical, physical, and microbiological methods in a Class III medical device environment.

The role requires a HLO/Bachelor's degree, strong leadership, and fluency in English and Dutch, with 3+ years of supervisory experience in regulated labs. On-site position with GMP/ISO13485 adherence.