Senior Quality Assurance Specialist

g2 Recruitment; Rotterdam; On-site; EUR 50,000 - 65,000; Full time

Benefits offered by this job

8% bonus

Travel allowance

Pension

26 days annual leave + 5.5 ADV days

Job summary

Senior QA Specialist role on-site near Rotterdam working for a market-leading medical device manufacturer. You will lead QA activities, ensure GMP compliance, manage CAPAs and GLP, and align with ISO 13485 standards while mentoring junior staff.

Fluent English is required; Dutch is beneficial. Start date around September–November 2026 for a permanent position with a competitive salary and benefits package including an 8% bonus, travel allowance, pension, and generous leave.

Qualifications

• Bachelor's degree in engineering or science required.
• Experience with QA, GMP, CAPAs and GLP.
• ISO 13485 knowledge essential.
• Independent work capability.
• Fluent English essential (Dutch beneficial).

Responsibilities

• Lead QA activities ensuring GMP compliance and GLP.
• Coordinate CAPAs and QA documentation across functions.
• Mentor junior QA staff and oversee training.
• Collaborate with engineering and manufacturing to ensure product quality.

Skills

QA Officer

GMP Compliance

CAPA & GLP

Independent Worker

Fluent English

Education

Bachelor's degree in engineering or science

Job description

Senior QA Specialist – On-Site role with a market-leading medical device manufacturer near Rotterdam.

Lead QA activities, ensuring GMP compliance, conducting CAPAs and GLP, and maintaining ISO 13485 alignment. Mentoring junior staff, coordinating cross-functional processes with engineering and manufacturing teams.

Fluent English required; Dutch beneficial.

Start date around September–November 2026. Permanent position with salary €4,500–€5,800 per month plus 8% bonus, travel allowance, pension, and 26 days annual leave + 5.5 ADV days.

• Bachelor's degree in an engineering or scientific discipline
• Background as QA Officer, Specialist, Quality Engineer, or similar
• Experience working on QA, documentation, GMP, CAPAs and GLP
• Experience in Medical Manufacturing sector + pharmaceuticals considered
• ISO 13485 essential
• Independent work capability
• Fluent English essential
• Dutch beneficial