Regulatory Affairs Specialist I

3 weeks ago

Raynham, United States Johnson & Johnson Full time

DePuy Synthes, part of Johnson & Johnson MedTech, is recruiting for a **Regulatory Affairs Specialist I **to support our Spine business. _This role is located on-site in Raynham, MA and will work a Flex/Hybrid schedule with three days of on-site and two days of off-site work _.

**About Johnson & Johnson**

**Key Responsibilities**:

- Provides independent regulatory guidance to product development teams in defining regulatory strategies, pre-marketing, and related submissions to support optimal timelines for new/modified product launches in the global market
- Leads the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers, including, but not limited to 510(k) submissions, IDE/IDE Supplements, PMA/PMA Supplements, Annual Reports, HDEs, IND/NDA Supplements, Design Dossiers/Change Notifications, and Technical Files.
- Guides conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials.
- Defines data and information needed for regulatory approvals.
- Develops labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations.
- Provide Regulatory Affairs support during internal and external audits.
- Plans schedules for delivery of supporting documentations required for regulatory submissions on a project and monitors project through completion.
- Assists in the development of improved and efficient processes practices for Regulatory Affairs processes.
- Represents Regulatory Affairs on cross-functional project teams, guiding and supporting product development teams on both US and international issues.
- Partners with other functions to define and generate data to assist with regulatory submissions.
- Review and provide regulatory authorization for Engineering Change Orders (ECOs).
- Respond to requests from foreign governments and/or distributors to prepare and submit documentation for marketing approvals in other countries, as well as provide routine regulatory information to associates and affiliates.

**Qualifications**:
**Required Qualifications**:

- Minimum of a Bachelor’s Degree **required **, Advanced Degree _strongly preferred _. Desired fields of study include science, engineering (e.g., biomedical, electrical, software, mechanical), business, legal, or similar.
- Minimum 1-2+ years’ of regulatory experience in a highly regulated industry, preferably in medical device or pharmaceutical. _Relevant internship experience may be considered _.
- Demonstrated intellectual capacity to identify, read, understand, and address global medical device regulations are required.
- Experience in the preparation and submission of US regulatory filings (e.g., 510(k), PMA) as well as European technical files and design dossiers is strongly preferred.
- Knowledge of US and European regulatory processes is preferred.
- Must have excellent written, verbal communication, and presentation skills.
- This position will be located in Raynham, MA, and may require up to 10% domestic/international travel.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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