CQV Engineer — Pharma Validation & Documentation Lead

Q-People; Antwerpen; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Attractive salary package

Extensive training package through Q-Academy

Work-life balance

Résumé du poste

Q-People in Antwerpen is looking for a validation specialist to develop and supervise validation operations in the pharmaceutical field. You will work closely with clients to ensure all validation strategies comply with quality standards.

The ideal candidate holds a master or bachelor degree in pharmacy, has at least one year of experience in a related industry, and is fluent in French with good English skills. An attractive salary package and work-life balance are offered.

Qualifications

• Master or bachelor degree in the pharmaceutical field.
• At least a year of relevant experience in the pharmaceutical, medical devices or diagnostics industry.
• GMP knowledge is essential.

Responsabilités

• Develop validation strategy (VMP) and plans in compliance with quality standards.
• Write validation protocols for projects.
• Initiate, execute, and supervise validation operations.
• Perform documentary verification and approval during projects.

Connaissances

Communication skills

Planning skills

Organization skills

Teamwork

GMP knowledge

Fluency in French

Good knowledge of English

Formation

Master or bachelor degree in the pharmaceutical field

Description du poste

Q-People in Antwerpen is looking for a validation specialist to develop and supervise validation operations in the pharmaceutical field. You will work closely with clients to ensure all validation strategies comply with quality standards.

The ideal candidate holds a master or bachelor degree in pharmacy, has at least one year of experience in a related industry, and is fluent in French with good English skills. An attractive salary package and work-life balance are offered.