Engineer

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

Job Title

CQV Engineer

Sector

Pharmaceutical / Medical Device Manufacturing

Role

The CQV Engineer is responsible for commissioning, qualification, and validation activities within a GMP manufacturing environment. The role focuses on hands‑on execution and documentation for secondary packaging systems, ensuring systems meet regulatory and internal requirements. The position reports to Validation & Compliance within Site Engineering.

Non‑Negotiable Requirements

• Degree in Engineering or related technical discipline
• Minimum 3 years of CQV experience in a pharmaceutical or medical device manufacturing environment
• Hands‑on commissioning and qualification experience in secondary packaging operations
• Experience with secondary packaging equipment using print and inspection systems
• Computerized Systems Validation (CSV) experience
• Experience creating GMP‑compliant CQV documentation
• Experience developing validation and commissioning plans
• Experience performing risk assessments and criticality assessments
• Experience executing IQ, OQ, and PQ activities
• Experience writing test protocols and validation reports
• Experience creating requirement traceability matrices
• Experience supporting engineering projects in a GMP environment
• Experience with Systech systems
• Experience with Cognex vision systems
• Experience working independently or with remote teams
• Experience supporting multiple project phases from design through validation

Practical Information

Location: Breda, The Netherlands

Start Date: ASAP

Work Model: Full time

Send your CV or inquiries to: [e-mail]

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing