Validation Engineer

Advanced Resource Managers; Kingston upon Hull; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading consultancy is seeking a Validation Engineer to ensure regulatory compliance and quality standards in the pharmaceutical sector. The role involves executing validation activities, providing technical leadership, and managing validation projects. Ideal candidates will have extensive experience in validation within GMP-regulated environments and a relevant engineering degree.

Qualifications

• 5+ years of experience in a similar validation role.
• Deep understanding of GMP and regulatory expectations.
• Skilled in the development of Master Validation Plans.

Responsibilities

• Execute validation/qualification activities in line with cGMP and company QMS.
• Author and report validation documentation including Validation Summary Reports.
• Serve as subject matter expert for Computerised System Validation.

Skills

GMP

Validation

Change Control

Education

Degree in Mechanical, Electrical, Chemical Engineering

Job description

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Lead Regulatory, Quality and Engineering Consultant @ Advanced Resource Managers -[phone] | [e-mail]

Our client is a specialist consultancy providing expert services to the pharmaceutical, medical device, and food supplement industries across the full product lifecycle.

As the Validation Engineer, you will play a critical role in ensuring all validation and qualification activities meet regulatory, safety, and quality standards. You'll work closely with cross-functional teams, provide technical leadership, and help shape validation strategies across equipment, facilities, utilities, and control systems.

Responsibilities:

• Execute validation/qualification activities in line with cGMP, EU Annex 11 & 15, and company QMS.
• Author and report validation documentation (URS, IQ/OQ/PQ, Validation Summary Reports).
• Serve as subject matter expert for Computerised System Validation aligned with GAMP 5 and 21 CFR Part 11.
• Manage validation projects and coordinate between key stakeholders.
• Review maintenance histories, lead investigations, support audits, and improve processes.
• Provide technical input to equipment design and commissioning plans.
• Ensure compliance with engineering, safety, and quality standards.

Requirements:

• 5+ years of experience in a similar validation role within a pharmaceutical or GMP-regulated environment.
• Degree in Mechanical, Electrical, Chemical Engineering, or equivalent experience.
• Deep understanding of GMP, validation requirements, and regulatory expectations.
• Skilled in Change Control and development of Master Validation Plans.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance and Engineering

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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