GMP QA Specialist — Validation, Compliance & Risk

SIRE LIFE SCIENCES; Breda; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical organization in Netherlands is looking for a QA Specialist to provide quality assurance support and oversight for equipment and automation validation. The role requires a Master's degree and at least 3 years of experience in a GMP environment. You will ensure compliance with GMP standards and guide teams on quality policies, contributing to risk management activities and supporting quality engineering. This is an essential position for maintaining high standards in product quality.

Qualifications

• 3+ years of experience in a GMP environment.
• Strong background in equipment and automation validation.
• Proven knowledge of GMP and computer compliance.

Responsibilities

• Perform QA support and oversight for equipment, automation, and IS validation.
• Review and approve validation documentation to meet standards.
• Provide guidance on quality policies and procedures.

Skills

Analytical skills

Communication

Decision-making

Collaboration

Education

Master’s degree in Engineering, Pharmaceutical Sciences, or equivalent

Job description

A leading pharmaceutical organization in Netherlands is looking for a QA Specialist to provide quality assurance support and oversight for equipment and automation validation. The role requires a Master's degree and at least 3 years of experience in a GMP environment. You will ensure compliance with GMP standards and guide teams on quality policies, contributing to risk management activities and supporting quality engineering. This is an essential position for maintaining high standards in product quality.