Job Description

Are you a meticulous professional with a passion for precision and quality?

A leading organisation in Central Scotland is seeking a dedicated Validation Engineer for a 12-month contract role, driven by recent and future expansion.

This is an exceptional chance to contribute to a dynamic team, ensuring the highest standards in product and process validation. Imagine working in a stimulating environment where your expertise is valued and your contributions make a tangible impact.

As a Validation Engineer, the primary responsibility will be to support the validation of equipment, processes, and systems to ensure compliance with industry standards and regulatory requirements. This involves developing and executing validation protocols, conducting risk assessments, and maintaining detailed documentation. The role demands a proactive approach, with a keen eye for detail and a commitment to excellence.

Candidates should possess a degree in Engineering, Life Sciences, or a related field, coupled with substantial experience in validation within a regulated industry, such as pharmaceuticals, biotechnology, or medical devices.

Proficiency in validation methodologies, including IQ, OQ, and PQ, is essential. Strong analytical skills, the ability to troubleshoot and resolve complex issues, and a thorough understanding of GMP regulations are also required.  Experience in Aseptic processing is very desirable for this role.

In addition to technical prowess, the ideal candidate will demonstrate excellent communication skills, both written and verbal, and the ability to work effectively within a team. A methodical mindset, combined with a proactive attitude, will ensure success in this role.

To find out more about this opportunity, please contact Lynsey today on (phone number removed) or send an up to date copy of your CV to (url removed)