Validation Manager

RBW Consulting; Manchester; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company is seeking a Validation Manager in Greater Manchester. The role involves leading validation activities for new products and processes, ensuring compliance with GMP standards, and supporting regulatory submissions. Ideal candidates will have a degree in a scientific discipline and at least 5 years of experience in validation within the pharmaceutical sector. This position offers a unique opportunity to shape validation processes in a fast-growing environment.

Qualifications

• Minimum 5 years’ experience in validation of products/processes within a pharmaceutical setting.
• Strong knowledge of GMP, GLP, MHRA, and HSE regulations.

Responsibilities

• Manage and deliver validation activities for new products/processes.
• Oversee validation documentation and ensure timely approvals.
• Support regulatory submissions and act as SME during audits.
• Provide hands-on training and development for staff.
• Coordinate with Site Managers and Northern Europe team.

Skills

GMP compliance

Regulatory knowledge

Communication skills

Organizational skills

Interpersonal skills

Proficiency in Microsoft Office

Education

Degree in a relevant scientific discipline

Tools

PrOFS

Job description

Validation Manager – Greater Manchester

We’re working with a leading pharmaceutical company entering an exciting phase of growth, with new product introductions, operational scale-ups, and expansions at their brand-new site. This is a unique opportunity to help launch a new facility while defining validation processes and ensuring robust GMP compliance.

As Validation Manager, you’ll lead validation activities for new products and processes, manage the validation lifecycle, and support regulatory submissions. You’ll also provide technical training, mentor staff, and collaborate with teams across Northern Europe to streamline validation and introduce innovative solutions.

This is a fantastic opportunity for a validation professional with a strong pharmaceutical background who is ready to lead, innovate, and make a lasting impact.

Key Responsibilities

• Manage and deliver validation activities for new products/processes in strict adherence to GMP and pharmacopeia standards.
• Oversee validation documentation (VMP, URS, DQ, IQ, OQ, PQ, PV) and ensure timely approvals.
• Support regulatory submissions and act as SME during audits.
• Provide hands‑on training and development for staff across the RP network.
• Coordinate with Site Managers and Northern Europe team to share best practices and streamline processes.
• Establish maintenance schedules and manage calibration/qualification for new equipment.
• Drive continuous improvement and contribute to new product development.

Requirements

• Degree in a relevant scientific discipline.
• Minimum 5 years’ experience in validation of products/processes within a pharmaceutical setting.
• Strong regulatory knowledge (GMP, GLP, MHRA, HSE).
• Excellent communication, organisation, and interpersonal skills.
• Proficiency in Microsoft Office and understanding of PrOFS.