Pharma Validation Engineer: Process & Equipment Excellence

Biopharma Careers; Arklow; On-site; EUR 45,000 - 65,000; Full time

Job summary

Servier Ireland is seeking a Validation Engineer within the Quality Validation team to coordinate, execute and report Process, Transport and Cleaning Validation activities across site operations. You will prepare and review IQ/OQ/PQ documentation, support equipment and facility qualifications, and ensure all validation activities align with site procedures and regulatory expectations.

The role requires GMP experience, strong writing and communication skills, and the ability to work

Qualifications

• Minimum 2-3 years validation experience.
• A Third level degree in a Scientific or Engineering Discipline or equivalent.
• A good knowledge of validation procedures and execution.
• Pharmaceutical experience
• Strong communication and organisational skills.
• Experience in a GMP regulated environment.
• Good IT skills
• Excellent writing skills

Responsibilities

• Coordinate, execution and reporting of Process, Transport and Cleaning Validation activities.
• Support equipment/system/facility/utility and laboratory qualification activities.
• Protocol preparation and report writing.
• Coordinate and report on cleaning monitoring, ongoing process verifications and equipment requalification activities.
• Execute cleaning verification activities.
• Support Industrial Transfers, Internal Transfers and Optimisations.
• Prepare, review and maintain IQ/OQ/PQ documentation for validation of equipment and systems.
• Investigate and resolve non-conformances and deviations associated with validation studies.
• Work with validation teams across departments to ensure compliance with site procedures.

Skills

Validation experience

GMP experience

Communication skills

Writing skills

IT skills

Education

Third level degree in Scientific or Engineering Discipline

Job description

Servier Ireland is seeking a Validation Engineer within the Quality Validation team to coordinate, execute and report Process, Transport and Cleaning Validation activities across site operations. You will prepare and review IQ/OQ/PQ documentation, support equipment and facility qualifications, and ensure all validation activities align with site procedures and regulatory expectations.

The role requires GMP experience, strong writing and communication skills, and the ability to work