Validation Engineer

Are you looking for a new role as a Validation Engineer? Do you have comprehensive knowledge in the areas of the validation of equipment, processes and test methods? If you are interested in working for a leading Medical Device manufacturer this could be the role for you!

The successful Validation Engineer will have the ability to execute and facilitate multiple validation projects, as well as being directly involved in the qualifications of facilities, utilities and equipment. You will also be overseeing the planning and communication of validation activities across the site.

This is offered initially on a 12 month contract basis working Mon-Fri 09:00-17:00.

Responsibilities:

• Author validation documentation including, but not limited to:
• Installation, Operational and Performance Qualification protocols and reports, Process Validation protocols and reports, and Protocol Discrepancies and Addenda; IQ/OQ/PQ.
• Prepare Equipment and Process validation protocols according to internal and external requirements.
• Execute qualification and process validation tests in accordance with approved protocols, procedures, and guidelines.
• Analyse validation test data to determine systems have met validation criteria.
• Write validation final reports that offer conclusions based on test results.
• Assure that all validation activities are performed in compliance with approved validation/qualification protocols, standard operating procedures (SOPs), and current regulatory requirements/guidelines.
• Has proficiency in more than one functional area (Equipment Qualification, Process validation, etc.)
• Planning/coordination validation activities including document approval and protocol execution.
• Reporting progress and escalating issues.
• Champion validation life cycle approach across site.
• Keep current on regulatory and quality requirements for regulated testing, qualification, and validation activities.

Experience / Qualifications:

• Bachelor's degree in Engineering or Science discipline.
• Previous experience working in industry.
• Previous experience of drafting and executing validation protocols and reports.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.