23I/KSPR - Product Registration Officer Job at Randox Laboratories
We are currently looking to employ an experienced and motivated Product Registration Officer to work within the Quality Assurance / Regulatory Department based in Kearneysville, USA.
The Role:
The Candidate:
Essential:
Desirable:
This is an excellent opportunity to join an innovative international company in a growing industry, which can provide career security and genuine advancement opportunities for those who show potential.
The Role:
- To assist with the worldwide registration of Randox Products.
- Prepare regulatory documentation, review, and update technical files and performance data to ensure compliance with national and international regulations and standards.
- Generate and submit registration files to obtain and maintain marketing authorisations for in-vitro diagnostic devices. Prepare and respond to questions for regulatory authorities.
- Work with departments to maintain the life cycle of documents for Randox Products. To assess the impact of changes to registrations and the updating of technical files following the implementation of changes.
- Creation and updating of technical files to compile with standards and assist with notifying of Competent Authorities and notified bodies.
- Perform detailed format reviews of the technical files to ensure consistency.
- Review and approval of product labelling (IFU).
- Provide regulatory support for customers, distributors, and OEM partners.
- Work with the QA & Regulatory teams to ensure regulatory compliance and licenses are maintained.
- Coordinate the legislation of registration documents.
The Candidate:
Essential:
- Educated to degree level in a Science or Engineering related discipline or relevant experience.
- Excellent communication skills (written and verbal), and the ability to communicate information in a concise manner.
- Excellent leadership skills and a high level of self-motivation.
- Ability to work methodically and reliably under pressure.
- Excellent attention to detail.
- Computer skills including Word, Excel, PowerPoint, Microsoft Outlook.
- Experience with interpretation of technical information and performance data.
- Flexible approach and willingness to work outside hours, if required.
Desirable:
- Experience of working in a highly regulated industry, e.g., ISO13485, IVDD 98/79/EC, IVDR 2017/746, 21 CFR 820 or similar standards.
- Experience in preparing technical files.
- Experience in a controlled manufacturing or analytical environment.
- Experience in registering IVD products and CDx products in US, Europe, China, and Japan.
This is an excellent opportunity to join an innovative international company in a growing industry, which can provide career security and genuine advancement opportunities for those who show potential.
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