Validation Engineer

14380Permanent Competitive Site Based Oxfordshire, United Kingdom Updated on: 06-03-2025

ROLE OVERVIEW

A leading pharmaceutical company based in the Oxfordshire area is seeking a Validation Engineer to join their dynamic team. This role offers the chance to leverage your technical and regulatory expertise in a rewarding environment. As the Validation Engineer, you will play a crucial role in ensuring the quality and compliance of pharmaceutical manufacturing processes.

KEY DUTIES AND RESPONSIBILITIES:

1. Conducting validation processes for equipment, systems, and cleaning procedures to ensure compliance with regulatory standards.
2. Managing validation projects from planning through execution and reporting, ensuring timely and budget-compliant completion.
3. Developing and managing Site Validation Master Plans and performing quality and compliance gap assessments.
4. Writing, reviewing, and approving validation protocols (IQ/OQ/PQ) and reports.

ROLE REQUIREMENTS:

1. Relevant degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a related field.
2. Proven industry experience in pharmaceutical validation processes, including GMP.
3. A working knowledge and practical experience with regulatory guidelines such as MHRA, FDA, and EMA standards.

Key Words:
Validation Engineer / Pharmaceutical Validation / GMP / Equipment Validation / Process Validation / Cleaning Validation / Computer System Validation / Regulatory Compliance / Validation Protocols / Data Analysis