CQV Engineer – GMP Validation Lead (Pharma/Med Devices)

Panda International; Breda; On-site; EUR 55,000 - 70,000; Full time

Job summary

A pharmaceutical manufacturing company located in Breda is seeking a CQV Engineer to oversee commissioning, qualification, and validation activities in a GMP environment. The ideal candidate will possess a degree in Engineering and at least three years of relevant experience. Responsibilities include executing documentation for secondary packaging systems and ensuring compliance with regulatory standards. This full-time position requires expertise in risk assessments, IQ/OQ/PQ activities, and supporting multiple project phases.

Qualifications

• Minimum 3 years of CQV experience in a pharmaceutical or medical device manufacturing environment.
• Hands-on experience in secondary packaging operations.
• Experience with creating GMP-compliant CQV documentation.

Responsibilities

• Responsible for commissioning and qualification activities within a GMP manufacturing environment.
• Executing and documenting secondary packaging systems to meet regulatory requirements.
• Supporting multiple project phases from design through validation.

Skills

CQV experience

Hands-on commissioning

Risk assessments

Test protocols writing

Working independently

Education

Degree in Engineering or related technical discipline

Tools

Systech systems

Cognex vision systems

Job description

A pharmaceutical manufacturing company located in Breda is seeking a CQV Engineer to oversee commissioning, qualification, and validation activities in a GMP environment. The ideal candidate will possess a degree in Engineering and at least three years of relevant experience. Responsibilities include executing documentation for secondary packaging systems and ensuring compliance with regulatory standards. This full-time position requires expertise in risk assessments, IQ/OQ/PQ activities, and supporting multiple project phases.