Validation Engineer – GMP Life Science & Cleanrooms

Network Scientific Ltd.; England; On-site; GBP 45,000 - 55,000; Full time

Job summary

Network Scientific Ltd. in Surrey, UK, is seeking a Validation Engineer to join a GMP Life Science environment focusing on clean rooms, biocontainment and laboratory setup for new laboratories and expansions.

You will lead validation activities across the full lifecycle, generating URS, VMP, VP, RTM, DQ, IQ, OQ and VSR, and provide detailed consultancy to stakeholders while ensuring regulatory compliance and high-quality documentation.

Qualifications

• Degree in a science or engineering field with GMP exposure.
• Experience delivering validation projects in Life Science environments.
• Familiarity with regulatory requirements for clean rooms and biocontainment.

Responsibilities

• Lead Projects through all stages of design and development
• Collaborate with end users, designers and contractors to meet timescales
• Provide consultancy on regulatory and engineering standards for clean room design
• Execute validation protocols at customer and vendor facilities
• Generate Quality Risk assessments
• Lead project meetings including site visits
• Create Validation Protocols for full validation life cycle (URS, VMP, VP, RTM, DQ, IQ, OQ, VSR)
• Review and maintain progress reports and budgets
• Implement continuous improvement to processes and documentation

Skills

GMP knowledge

Clean room experience

Project delivery

Regulatory compliance

Documentation accuracy

Confidentiality

Attention to detail

Education

Scientific degree or higher

Job description

Network Scientific Ltd. in Surrey, UK, is seeking a Validation Engineer to join a GMP Life Science environment focusing on clean rooms, biocontainment and laboratory setup for new laboratories and expansions.

You will lead validation activities across the full lifecycle, generating URS, VMP, VP, RTM, DQ, IQ, OQ and VSR, and provide detailed consultancy to stakeholders while ensuring regulatory compliance and high-quality documentation.