Validation Engineer - Injection Moulding
Key Responsibilities:
1. Write and execute process validation protocols and reports for new product introductions and revalidations due to process/material improvements utilizing scientific/technical knowledge.
2. Develop and implement solutions to sustain and improve the QMS.
3. Maintain and support compliance to ISO 13485 and ISO 14001 systems standards.
4. Participate in the site change control, ensuring that all changes to validated processes are effectively identified and implemented.
5. Generate risk assessments, covering cleaning, validation, and process.
6. Review and execute Factory Acceptance Testing and Site Acceptance Testing protocols.
7. Directly support GMP and regulatory audits.
8. Prepare and deliver training modules as required.
9. Perform data analysis and make informed decisions/recommendations around conclusions reached from data analysis.
10. Support continuous improvement through Lean Six Sigma methodologies.
11. Execute/develop change controls.
12. Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues e.g., FMEA, Fishbone diagrams, 5 why’s etc.;
13. Implement subsequent corrective action through the change management system.
14. Participate/lead cross-functional teams including liaising with vendors on projects.
Qualifications & Key Attributes:
1. Third level qualification in Engineering, Polymer Science, or equivalent Manufacturing experience.
2. Experience in statistical analysis (Minitab)/SPC/validations.
3. Excellent interpersonal, communication, influencing, and facilitation skills.
4. A minimum of 2 years’ experience as a Validation Engineer within an Injection moulding or medical manufacturing environment.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Medical Equipment Manufacturing
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