Validation Engineer - Permanent

Join a dynamic Quality Assurance team in Co. Galway, as a pivotal Validation Engineer to support on there new and exciting projects!

This role places you at the forefront of ensuring excellence in validation activities within a prestigious pharmaceutical setting. You will report to the Director of Quality, your Validation expertise will be instrumental in reviewing and issuing validation protocols and reports, as well as coordinating the execution of various validation activities, including process, cleaning, equipment, and computer qualifications.

As a Validation Engineer, you will play a critical role in shaping the Validation Master Plan, managing validation requirements for the client and third-party suppliers, and ensuring compliance with EU regulatory standards. Your contributions will directly impact the quality and safety of products, making your role essential to the companys success.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Validation Engineer will be varied however the key duties and responsibilities are as follows:

1. Oversee the preparation and review of the Validation Master Plan, focusing on process and cleaning.
2. Coordinate validation execution in collaboration with Production, Quality Control, and R&D teams.
3. Lead cross-functional teams, providing expertise in resolving technical issues and contributing to regulatory and customer audits.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the Validation Engineer, we are looking to identify the following on your profile and past history:

1. A Bachelor of Science or Engineering degree, with a preference for a focus in a Scientific Discipline.
2. Proven experience in a similar validation role within the pharmaceutical industry.
3. A working knowledge and practical experience with process and cleaning validation, as well as internal and external audit participation.

Key Words:

Validation Engineer / Quality Assurance / Pharmaceutical / Validation Protocols / Validation Master Plan / Process Validation / Cleaning Validation / EU Regulatory Compliance / HPRA / USFDA / Cross-Functional Leadership / Audit Participation / Risk Assessment / Non-Conformance Management

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications for any applicant who fulfills the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.