GMP QA Specialist - Equipment & Packaging Validation

Talentmark; Breda; On-site; EUR 80,000 - 84,000; Full time

Job summary

A leading pharmaceutical company is seeking a QA Specialist (GMP) in Breda, Netherlands. In this role, you will provide quality oversight for equipment and automation validation, ensure compliance with GMP regulations, and collaborate with engineering and operational teams. The ideal candidate will have a Master's degree, 5–8 years of experience in a GMP-regulated environment, and strong experience with equipment and validation processes. This is a full-time position with a gross annual salary of €80,000–€84,000.

Qualifications

• 5–8 years of experience in a GMP-regulated pharmaceutical environment.
• Proven experience with labeling and packaging equipment validation.
• Strong experience with equipment and automation validation.

Responsibilities

• Provide QA oversight for validation of equipment, automation, and information systems.
• Review and approve validation documentation in compliance with GMP and regulatory requirements.
• Support the introduction and validation of labeling and packaging equipment.
• Collaborate with engineering and validation teams to define testing strategies.

Skills

Strong analytical skills

Excellent communication skills in English

Experience with equipment and automation validation

Knowledge of GMP regulations and validation guidelines

Education

Master’s degree in Engineering, Pharmaceutical Sciences, Process Technology

Job description

A leading pharmaceutical company is seeking a QA Specialist (GMP) in Breda, Netherlands. In this role, you will provide quality oversight for equipment and automation validation, ensure compliance with GMP regulations, and collaborate with engineering and operational teams. The ideal candidate will have a Master's degree, 5–8 years of experience in a GMP-regulated environment, and strong experience with equipment and validation processes. This is a full-time position with a gross annual salary of €80,000–€84,000.