Validation Specialist – Pharma

Network Scientific Ltd.; England; On-site; GBP 37,000 - 45,000; Full time

Job summary

An established industry player is seeking a Validation Specialist to enhance their production team in Guildford. This permanent, full-time role offers the chance to engage in production and process validation, ensuring compliance with cGMP guidelines. You will be responsible for supporting new products and processes, providing technical expertise, and driving continuous improvement initiatives. Join a dynamic environment where your skills will directly contribute to the success of specialist pharmaceuticals. If you're ready for a new challenge and have a passion for quality assurance, this opportunity is perfect for you.

Qualifications

• Degree level education or equivalent in Pharmaceutical Production.
• Strong experience in troubleshooting and continuous improvement.

Responsibilities

• Responsible for validation activities to support new products/processes.
• Support QA team in generating documentation for validation.

Skills

Troubleshooting

Continuous Improvement

Production Validation

Process Validation

Lean Six Sigma

Education

Degree in relevant discipline

Job description

Do you have experience of production and process validation? Are you looking for a new challenge with a leading Pharmaceutical Manufacturer?

A manufacturer of specialist pharmaceuticals is currently seeking a Validation Specialist to join the production team at their site in Guildford. The role will involve taking on production and process validation responsibility for the production team. This is a permanent, full-time role. Predominantly standard day shifts Monday to Friday, with a requirement for occasional weekend or night shifts. £37K - £45K

Role Overview

• Responsible for validation activities to support new products/processes in compliance with cGMP and all relevant guidelines.
• Supporting the QA team to generate documentation (IQ, OQ, PQ, RQ etc.)
• Provide technical expertise and troubleshooting issues related to production and processes and identify areas for improvement.

Requirements

• Educated to Degree level or equivalent in relevant discipline or equivalent relevant experience in Pharmaceutical Production.
• Strong experience in troubleshooting and continuous improvement with respect to processes used in cGMP Production.
• Previous experience in production and process validation specifically is essential (as opposed to QC/Method Validation).
• Knowledge of and experience with Lean Six Sigma and similar methodologies is highly beneficial.

For more information, please contact Louis Williams.