CQV Engineer

1. Job Title

CQV Engineer (GMP)

---

2. Sector

Pharmaceutical / Medical Device Manufacturing

---

3. 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.

---

4. 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

---

5. Essential Requirements

• 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

---

6. Desirable Requirements

• 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

Interested or know someone who might be?
Send your CV or inquiries to e.cabral@panda-int.com