At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.

DESCRIPTION OVERVIEW

Preparation and execution of validation protocols according to the Validation master plans and schedules in Process Validation (including Performance Qualification, product hold time and transport studies), Equipment Qualification, Cleaning Validation, Computer Systems Validation, Spreadsheet Validation and execution and reporting of temperature profile mapping for Quality Critical equipment
Conduct periodic lifecycle reviews for each of the validation disciplines.
Support Improvement projects with technical input and participating in problem solving teams (e.g CAPA, Quality Event, Kaizen).

EXPERIENCE REQUIRED

• Flexibility to work varied hours as needed – although it is not envisaged that this will be a regular or frequent occurrence.
• Minimum of 2 years’ experience of validation or process engineering roles in the pharmaceutical or other regulated industry
• Knowledge of GMP and its application in validation and change management and improvement processes, ability to learn new regulations.
• Ideally experience of working in an environment employing some elements of lean management, but not essential