Sr. Regulatory Affairs Specialist

• Be a part of mission-driven work in a critical, growing field
• Company is backed by major investment and positioned for long term growth

About Our Client

My client is a global MedTech leader specializing in fertility treatment technologies, formed by integrating several of the most respected brands in reproductive health, laboratory technology, and fertilityfocused medical devices.

Job Description

They key responsibilities of the Senior Regulatory Affairs Specialist are:

• Develop and execute regulatory strategies to support product development, submissions, and postapproval activities.
• Prepare, review, and submit regulatory filings, including but not limited to INDs, NDAs, BLAs, 510(k)s, IDEs, supplements, amendments, and annual reports, as applicable.
• Serve as a primary regulatory contact for internal stakeholders, providing clear guidance on regulatory requirements, risks, and timelines.
• Interface with regulatory authorities (e.g., FDA) to manage inquiries, meeting requests, and formal correspondence.
• Ensure compliance with applicable U.S. and international regulations, guidance documents, and standards.
• Support labeling development and review to ensure regulatory compliance and alignment with approved claims.
• Contribute to regulatory impact assessments related to product changes, manufacturing updates, quality events, and lifecycle management activities.
• Partner crossfunctionally with Quality, Clinical, R&D, Manufacturing, and Commercial teams to support regulatory objectives.
• Monitor regulatory intelligence and assess potential impacts of changing regulations on existing and future products.
• Assist in the development, maintenance, and improvement of regulatory processes, procedures, and documentation.
• Support inspections, audits, and regulatory commitments, as needed.
• Mentor junior regulatory team members and provide subjectmatter guidance when appropriate.

If interested, please apply using the link below. Qualified applicants will be contacted 24-48 hours upon submittal.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.


The Successful Applicant

The successful Senior Regulatory Affairs Specialist will have:

• Bachelor's degree in a scientific, engineering, or healthcarerelated discipline (required); advanced degree preferred.
• 6+ years of progressive experience in Regulatory Affairs within a regulated healthcare environment (pharmaceutical, medical device, biologics, or combination products).
• Demonstrated experience preparing and managing regulatory submissions to the FDA and/or international regulatory bodies.
• Strong working knowledge of applicable FDA regulations (e.g., 21 CFR) and relevant international standards.
• Excellent written and verbal communication skills, with the ability to clearly convey regulatory concepts to diverse audiences.
• Proven ability to manage multiple priorities, meet deadlines, and work effectively in a fastpaced environment.
• High attention to detail, strong organizational skills, and sound problemsolving abilities.
• Ability to work independently while collaborating effectively within crossfunctional teams.

What's on Offer

My client can offer the following for the Senior Regulatory Affairs Specialist:

• Competitive Base Salary
• Strong Benefits and Company 401k Matching Program
• A collaborative environment built around innovation, precision, and supporting clinicians at every critical step of the ART process.
• Join an organization backed by major investment and positioned for long-term growth
• Stability and Scale with room for innovation

Contact

Daniel Hall

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JN-042026-7003694