Regulatory Affairs Project Manager at DEKA Research & Development

Manchester, New Hampshire, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Sep, 26

Salary

0.0

Posted On

14 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Strategy, FDA Submissions, 510(k), PMA, IDE, CE Marking, Clinical Trial Design, eSTAR, UDI, Post-market Reporting, ISO 13485, MDSAP, Quality Management Systems, Technical Writing, Project Management, Regulatory Compliance

Industry

Biotechnology Research

Description

DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to contribute to a dynamic, medical device research and development environment. The individual in this high visibility role will have a significant and direct impact on the success of the innovative life science devices that DEKA develops. The person in this role will formulate and execute regulatory strategies to deliver FDA approval or clearance as well as international approvals including CE Marking. How you will make a difference as a Regulatory Project Manager: Work in close association with customers and development teams to define and execute regulatory approval and clearance programs, including establishing regulatory requirements and leading the preparation and submission of 510(k)s, PMAs, IDEs, Technical Files, and other international dossiers Provide leadership and guidance to R&D in developing successful regulatory strategies across the entire product life cycle Mentor regulatory affairs staff, as well as internal cross-functional partners, on effective regulatory strategies and tactics Lead FDA interactions including in-person meetings, teleconferences, written submissions and other Agency engagements as needed Participate in the design and conduct of clinical trials, and assist in obtaining and maintaining the appropriate regulatory approvals from the FDA, IRBs and/or Ethics Boards Continually improve internal regulatory processes and procedures to increase efficiency and reduce time to market while maintaining the highest levels of compliance Skills you will need to be successful: BS in a technically related field Minimum of 5 years direct work experience in a medical device, drug or biologic regulatory role with demonstrated success in obtaining product approvals/clearances Experience in direct FDA interactions including premarket notifications, IDE’s, Q-submissions and participation in face-to-face meetings Strong written and verbal communication skills Demonstrated ability to continually balance priorities in a dynamic and fast-paced environment Expertise in current FDA processes including the eSTAR submission tool, establishment registration and listing, UDI, product labeling, and post-market reporting including MDR’s and Field Action Reporting Experience in Medical Device Quality Regulations including Quality Management Systems Regulations (QMSRs), ISO 13485, and MDSAP Demonstrated ability in expanding regulatory organization capabilities Experience with drug, biologic and combination product approvals a plus RAC certification a plus About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

Responsibilities

Formulate and execute regulatory strategies to obtain FDA and international approvals for innovative medical devices. Lead interactions with the FDA and collaborate with R&D teams to manage the product life cycle and clinical trials.