Senior CQV Engineer – Aseptic Fill & GMP Validation

EFOR; Noord-Brabant; On-site; EUR 90,000 - 130,000; Full time

Job summary

EFOR, a world-leading animal health production and R&D site in the southeast Netherlands, is seeking a senior CQV Engineer to ensure the excellence of aseptic filling line operations and capital projects.

You will lead commissioning, qualification and validation activities for filling lines, packaging systems and related equipment, developing, reviewing and executing IQ/OQ/PQ protocols in line with GMP requirements.

Qualifications

• Bachelor’s or Master’s degree in Engineering, Life Sciences, or related field.
• Minimum 7 years of hands-on CQV experience in pharmaceutical or animal health environments.
• Strong expertise in aseptic filling lines and associated equipment is a plus.
• Excellent communication, documentation, and problem-solving skills.

Responsibilities

• Lead commissioning, qualification, and validation activities for filling lines, packaging systems, and related equipment.
• Develop, review, and execute protocols (IQ, OQ, PQ) and validation reports in accordance with GMP requirements.
• Drive cross-functional collaboration with engineering, production, quality, and project management teams.
• Identify and resolve technical issues throughout project phases; ensure timely project delivery.
• Mentor and guide junior engineers in CQV execution and best practices.
• Maintain strict compliance with regulatory standards (EU GMP, FDA).

Skills

CQV engineering

Commissioning

Validation

IQ OQ PQ

GMP standards

Regulatory compliance

Leadership

Documentation

Cross-functional

Education

Bachelor’s degree in Engineering

Master’s degree

Job description

EFOR, a world-leading animal health production and R&D site in the southeast Netherlands, is seeking a senior CQV Engineer to ensure the excellence of aseptic filling line operations and capital projects.

You will lead commissioning, qualification and validation activities for filling lines, packaging systems and related equipment, developing, reviewing and executing IQ/OQ/PQ protocols in line with GMP requirements.