Senior Regulatory Affairs Specialist
What you need to know
Do you want to work for a leading innovative Medical Device Company in the West? Continue to read if so…
This company is pursuing highly differentiated medical devices that are designed to address unmet clinical needs and engineered to the most demanding requirements. This key growth strategy leverages the combination of the Company’s expertise in proprietary surface technologies, along with enhanced device design, development and manufacturing capabilities. The Company mission remains to improve the detection and treatment of disease.
This Senior Regulatory Affairs Specialist is responsible for coordinating, preparing, and maintaining regulatory submissions on a global level including European CE-marking and US FDA submissions.
This is a Permanent role
Location: Ballinasloe, Galway County, Ireland
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Key duties & responsibilities include:
- Evaluates potential global regulatory pathways for various projects for EU, US and International product launches / product enhancements. Identifies guidance documents, international standards, consensus standards and assists teams with their interpretation.
- Provides technical guidance and regulatory training/mentoring to cross-functional teams, maintaining and enhancing cross-functional team relationships, identifying relevant standards and guidance documents that affect business and products.
- Prepares regulatory submissions to regulatory authorities and/or distributors (including the FDA, Notified Bodies, Health Canada and other regulatory authorities).
- Maintains expertise in worldwide regulatory requirements, with an emphasis on MDR; establishes and maintains positive relationships with regulators.
- Interacts directly with international regulatory agencies on products / projects at reviewer level. Interacts with various levels of management, external agencies and companies. Works with engineers and technical experts to resolve potential regulatory issues and questions from Regulatory Agencies
- Provides support for commercialized products as necessary by reviewing labelling, promotional materials, and product and documentation changes per policy and procedure.
- Maintains and enhances cross-functional team relationships. Provides technical guidance and regulatory training / mentoring to other Regulatory Affairs employees and cross-functional teams.
- Participates in and assists with Notified Body Audits, MDSAP, FDA facility inspections, and other governmental inspections, as directed.
- Performs other related duties and tasks, as required.
What are we looking for?
- An Engineering or Quality Assurance Degree or equivalent experience.
- A minimum of eight (8) years within a Medical Device or regulated environment with at least five (5) of those years working as a Regulatory Specialist
- Demonstrable detailed working knowledge of the medical device industry and the regulatory environment in which the business operates including European (MDD and MDR), FDA, Health Canada, and other International Regulatory requirements
- An analytical approach to problem solving
- A self-starter that applies their own initiative in most situations
- A good team player, who works well in a small team environment, must be able to work effectively with peers in other departments.
- A good communicator who can easily convey his/her standards and requirements across all levels in the organisation and demonstrate confidence and presence in front of external regulatory body personnel.
- Displays the highest levels of integrity and a demonstrated ability to influence his/her peers.
- Attention to detail and ability to stay connected to multiple projects simultaneously.
Benefits: This company offers a competitive compensation and benefits package, including a bonus program, Defined Contribution Pension with employer match, employee stock purchase plan and stock options.
Apply for this job now or get in touch with Aoife at email@example.com