Validation Engineer - Sterilization & Life Sciences

Sterigenics; Alfreton CP; On-site; GBP 32,000 - 54,000; Full time

Benefits offered by this job

34 days holiday (26 + 8 Bank Holiday)

Medicash Health Plan

Company pension scheme

Life Assurance — cover of 4 times your

Employee Assistance Programme (EAP)

Cycle to work scheme

Job summary

Sterigenics söker en Associate Validation Engineer i Somercotes, UK, för att stödja planering och genomförande av valideringsaktiviteter i en reglerad miljö. Du kommer samarbeta med Operations, Engineering, Quality, och externa kunder för att leverera valideringsprogram i enlighet med regulatoriska krav.

Rollens ansvar omfattar utveckling och dokumentation av valideringsprotokoll, rapporter och arbetsinstruktioner samt kalibrering och årlig omkvalificering av utrustning.

Qualifications

• Experience in regulated Medical Devices, Pharmaceuticals, Life Sciences, Healthcare or Sterilisation.
• Experience writing and executing validation protocols.
• Ability to work in operational areas and handle validation samples and equipment.
• Strong IT skills including data analysis and report writing.
• Knowledge of Quality Management Systems.

Responsibilities

• Review customer and EAS-supplied validation protocols for feasibility and compliance.
• Prepare validation protocols, reports and associated technical documentation.
• Coordinate and execute validation studies, including scheduling and sample management.
• Collect, organise and analyse validation data to support objectives.
• Prepare validation work instructions and supporting documentation for personnel.
• Assist with validation calibration activities and equipment requalification programs.
• Maintain accurate, compliant validation records and update status in systems.
• Collaborate with Engineering and Maintenance teams on IQ/OQ/PQ protocols.

Skills

Regulated industry experience

Validation protocols

Data analysis

Documentation

Tools

Laboratory equipment handling

Job description

Sterigenics söker en Associate Validation Engineer i Somercotes, UK, för att stödja planering och genomförande av valideringsaktiviteter i en reglerad miljö. Du kommer samarbeta med Operations, Engineering, Quality, och externa kunder för att leverera valideringsprogram i enlighet med regulatoriska krav.

Rollens ansvar omfattar utveckling och dokumentation av valideringsprotokoll, rapporter och arbetsinstruktioner samt kalibrering och årlig omkvalificering av utrustning.