Validation Consultant (Pharmaceuticals)

TL;DR

Validation Consultant (Pharmaceuticals): Supporting validation activities for a pharmaceutical client project, including IQ/OQ and PQ documentation for equipment in an R&D pilot plant with an accent on governance integration, technical validation planning, and reporting. Focus on validating mixers and fillers, coordinating stakeholders in the UK and Slovakia, and leading validation plans across multiple projects.

Location: Hybrid in Surrey, United Kingdom, with 2 days onsite and travel to Slovakia required

Company

hirify.global provides engineering, project delivery, and technical consultancy services for pharmaceutical and other regulated industries.

What you will do

• Provide specialist validation support for a pharmaceutical client project.
• Integrate existing programme governance structures and working practices.
• Create and review IQ/OQ and PQ documentation for equipment in an R&D pilot plant in Slovakia.
• Work with stakeholders across the UK and Slovakia.
• Generate validation reports and lead or support validation plans.

Requirements

• Previous validation experience in a pharmaceutical, medical device, or R&D environment.
• Experience delivering validation across multiple projects.
• Experience with mixers and fillers.
• Ability to work hybrid in Surrey and travel to Slovakia.
• Strong technical competence and the ability to work efficiently and safely.

Culture & Benefits

• Six-month contract engagement.
• Outside IR35 contract arrangement.
• Hybrid working with two days onsite.
• Exposure to a cross-border pharmaceutical R&D pilot plant project.