S
Synergy Sterilisation (M) Sdn Bhd
Validation Technician
Skills
Performance ManagementCompliance
1 month ago
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Important information
Contract type:
Permanent
Location:
Kuala Ketil, Kedah, Malaysia
Work mode:
Onsite
Published on:
22 September 2026
What they need
- Works as directed by direct Supervisor to facilitate and support Customer EO qualifications within the EO Technical department.
- Carries out all aspects of their role and associated documentation in compliance with STERIS Quality Management System, ISO11135, ISO13485 and FDA regulatory requirements while adhering to GMP and GDP requirement. Complies with local and global procedures.
- Reviews qualification batch records for compliance to GDP and GMP, demonstrating a high level of attention to detail. Follows up with Operations to address and close out on any batch record queries within agreed timelines.
- Provides administration support to the EO Tech Team. Completes filing and archiving of qualification batch records and supporting EO qualification documentation.
- Sets and agrees annual GPS performance objectives with direct Supervisor. Actively participates in performance management reviews in line with STERIS corporate requirements and timelines.
- Actively participates in Team projects as agreed with direct Supervisor.
- Performs according to the guidelines outlined in the STERIS Code of Business Conduct. Supports STERIS AST business imperatives of Safety, Quality, Customer Focus, Innovation, Sustainability and Lean.
- Collaborates with all STERIS employees, Customers, auditors, and visitors to the site in a professional, constructive, and respectful manner. Encourages open communication providing timely and accurate responses.
- Complies with Health and safety polices & procedures, reports any concerns, potential risks or hazards to the Health and Safety representative so appropriate action can be taken.
- Other site-specific duties and/or responsibilities as assigned by direct Supervisor.
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