Senior QA: GMP Validation & PASX Master Data (Hybrid)

Orion Group; Breda; Hybrid; EUR 45,000 - 60,000; Full time

Job summary

A leading pharmaceuticals consulting firm is seeking a Senior Associate QA for a hybrid role based in Breda. This position focuses on validation and quality oversight in a multinational environment. The role requires a MBO or Bachelor’s degree and at least 3 years of experience in the pharmaceutical industry. Candidates should have strong GMP knowledge and effective communication skills. This is a 12-month initial contract with the possibility of extension.

Qualifications

• 3 years of relevant experience in the pharmaceutical or medical device industry.
• Experience in Equipment and Automation Validation.
• Fluency in English.

Responsibilities

• Perform QA oversight for validation of equipment and packaging qualification.
• Provide quality support for testing strategies and quality investigations.
• Manage client’s device responsibilities ensuring GMP regulations.

Skills

Relevant experience in the pharmaceutical industry

GMP knowledge

Analytical skills

Effective communication

Attention to detail

Change Control experience

Education

MBO or Bachelor’s degree in Life Sciences

Job description

A leading pharmaceuticals consulting firm is seeking a Senior Associate QA for a hybrid role based in Breda. This position focuses on validation and quality oversight in a multinational environment. The role requires a MBO or Bachelor’s degree and at least 3 years of experience in the pharmaceutical industry. Candidates should have strong GMP knowledge and effective communication skills. This is a 12-month initial contract with the possibility of extension.