About the Company
Our public sector client are looking for a Validation Specialist to work on a 12-month contract. The Validation Specialist will lead the validation processes required to conduct clinical research for a medical device clinical trial. This role offers Hybrid opportunity and flexible hours.
About your new job as a Validation officer
- Support the lab and research centre on validation needs, ensuring quality assurance for clinical research programs.
- Lead all validation processes
- Coordinate validation and qualification activities with internal teams and external vendors using a risk-based approach.
- Develop user requirements, technical specifications, and validation reports, ensuring regulatory compliance.
- Maintain validation processes in collaboration with QA to ensure studies meet Good Clinical Practice (GCP) and legislative standards.
- Ensure compliance with GCP, ISO 14155, GDPR, and related requirements.
- Deliver validation training to unit staff as needed.
- Monitor and ensure systems remain validated per SOPs in coordination with the Quality Manager.
- Manage validation change control
- Drive continuous improvement for validation processes.
- Support procurement activities, regulatory inspections, and internal audits.
- Assist with non-conformance investigations and corrective actions.
- Take on additional tasks to support operations
What skill/experience you need
- Engineering degree preferred
- Project management skills
What’s on offer
- 12 month Contract
- 35 hours per week
- Hourly rate DOE
- Flexible working available
What’s next
- Apply now by clicking “Apply Now” or contact me at 021 484 7135
- Or if the job isn’t quite right but you are looking for something similar, please get in touch.
