- Minimum BSc/BEng degree in a science or technical discipline with a relevant postgraduate qualification a distinct advantage
- Have completed post-qualification quality and regulatory training
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- Experience of implementing and maintaining ISO 13485
- Experience of hosting regulatory body notified body and customer audits
- Interpersonal skills and professional skills to interact at all levels including senior management, contractors and colleagues
- People management and supervisory experience
- Experience of ICH E6 GCP requirements would be an advantage
- Strong problem-solving and analytical skills
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Regulatory Affairs Manager - Ennis, Ireland - Vitalograph
1 week ago
Description
Benefits:
Company contributed pension
Private Health Insurance
Educational assistance programme
Development & progression opportunities
Vitalograph is the world's leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and advanced high-reliability equipment and software systems used in respiratory end-point clinical drug trials. We design and manufacture respiratory diagnostic devices, software, and consumables for healthcare professionals, for almost 60 years, and serve customers in over 100 countries. Headquartered in the UK, Vitalograph has operations in Ireland, Germany and the USA.
We now have an excellent opportunity available for a 'Regulatory Affairs Manager' in our facility in Ennis. With over 60 years in business and stability in the market, now is a very exciting time to join our expanding organisation.
Responsibilities as a Regulatory Affairs Manager:
Manage RA personnel
Foster and champion a regulatory culture within the business
Ensure that relevant global Regulatory Compliance requirements are identified, defined, documented, implemented, complied with, and sustained, including product safety requirements for the markets served
Ensure compliance with the following medical device & software quality requirements;
o EU Medical Device Directive and Medical Device Regulation guidelines and associated QSRs, such as the MEDDEVs
o ISO13485 Medical Device QMS
o MDSAP program member Quality System Regulations & associated documents
o US FDA 21 CFR Part 11 guidance
o ICH E6 GCP
o Other jurisdictional QSRs as related to Regulatory submissions
Facility & device registering, licencing and device change management etc., within applicable jurisdictions, including supporting licence holders with documentation etc. Assure conformity of devices is appropriately checked, in accordance with the documented QMS under which the devices are manufactured, before a device is released
Ensure technical documentation and the EU declaration of conformity are drawn up and kept up to date
Ensure that post-market surveillance obligations, including Reporting obligations, are complied with in accordance with the various regulations and or directives
Host Regulatory Inspections, Notified Body and customer onsite or remote audits
Prepare and or support Regulatory filings;
o CE Marking submissions for MDD and MDR
o US FDA submissions
o Notified Body registrations
o ROW registrations
o Oversight of AE or related Reporting to Regulatory Authorities
Maintain the product and establishment registrations
Support Clinical Trial Teams and Sponsors regarding device conformity and registration queries
Maintain regulatory oversight, plan and implement change programs to ensure continued compliance
Identify and maintain key essential quality KPIs including regular reporting of quality metrics and issues
Be the site regulatory representative on design teams including risk management approvals, NPI and design transfer
Participate in and give training on regulatory matters
Prepare and submit annual plans with focussed targets and associated budget
Requirements as a Regulatory Affairs Manager::
