Validation Lead Consultant

Russell Taylor Group Ltd; Manchester; On-site; GBP 150,000 - 200,000; Full time

Job summary

A leading biotechnology firm in Manchester seeks a Validation Lead Consultant to oversee validation activities across various departments. The ideal candidate will have a MA or PhD in Life Sciences, IT, or Engineering, along with 10+ years of management experience in Biotech/Pharma. This role offers a chance to lead high-value projects in a supportive organization committed to innovation and employee growth.

Qualifications

• 10+ years of management experience in Biotech/Pharma.
• Strong system validation and QMS experience.
• 5+ years of IT experience with software or system implementation exposure.

Responsibilities

• Lead validation activities across Manufacturing, Engineering and Technology departments.
• Oversee equipment validation from procurement to installation.
• Ensure compliance with ISO standards.

Skills

Management experience in Biotech/Pharma

System validation

Project management

Cross-functional collaboration

IT experience with software implementation

Education

MA or PhD in Life Sciences, IT or Engineering

Job description

Validation Lead Consultant

Location: Manchester (full time on site)

Working Hours: Mon - Fri (08:00 - 16:00)

Contract term: 11 months

Salary: £750/day

About the Role

• Lead validation activities across Manufacturing, Engineering and Technology departments managing teams *circa* 8 people and third-party vendors.
• Collaborate with Manufacturing Project Manager, Technology Adaption Manager and Global Strategic Project Leads.
• Oversee equipment validation from procurement to installation and maintenance.
• Support implementation of equipment from GLP lab equipment through to GMP Manufacturing equipment, supporting scale‑up capabilities.
• Ensure compliance with ISO 9001, ISO‑O14001 and ISO 4001 standards.
• Prepare URS, IQ, OQ, PQ and VMP documentation.
• Coordinate with IT departments for finalisation of GAMP assessments, software implementation and GDPR requirements.
• Lead engagement with Engineering teams regarding organisation of PAT testing and 6‑monthly/annual maintenance programmes.
• Maintain CAPEX assessments in collaboration with the Global Project Leads.

About You

• MA or PhD in Life Sciences, IT or Engineering.
• 10+ years of management experience in Biotech/Pharma.
• Strong system validation and QMS experience.
• 5+ years of IT experience with software or system implementation exposure.
• Background in research, biometrics, QC, analytical development or parenteral/solid dose manufacturing.
• Proven leadership, project management and cross‑functional collaboration skills.

Why Join?

You will be part of a supportive, forward‑thinking organisation committed to innovation, patient impact and employee growth. This is a fantastic opportunity to lead high‑value projects while shaping validation excellence across a global biotech environment.

Apply now to make a meaningful difference in brain health innovation.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us.