Manager, Regulatory Affairs

Overview

Responsible for the day-to-day leadership and operational management of the Regulatory Affairs function. This role oversees Regulatory Affairs personnel and ensures effective execution of U.S. and international regulatory activities, including regulatory submissions, inspections and audits, recalls, licensing, labeling and promotional review, quality system documentation, risk management, and design control support. Ability to travel up to 20% of time to MTF locations and to suppliers as required

Monday through Friday 8:15am to 4:30pm

Salary Range : $99,000- $125,000/yr.

Responsibilities

• Lead, coach, and develop Regulatory Affairs staff, including staffing plans, performance management, training, and competency maintenance. Also performs active management and observations of staff for compliance with regulations and process efficiencies.

• Assist in managing the budget for Regulatory Affairs department, including salaries, benefits, external vendors/consultants, supplies, services and internal expenses. Responsible for formulating/submitting budgets and managing to expense within budget requirements. Tracks monthly "budget to actual" performance.

• Oversee and assist in the preparation, submission, and maintenance of U.S. and international regulatory filings (FDA, CE Marking, Canada, Australia, and other global markets).

• Ensure maintenance of all applicable licenses, accreditations (AATB), and ISO 9001 / 13485 certifications.

• Participates in the development of regulatory strategies and pathway to support the regulatory designation of new products and tissues.

• Serve as a primary regulatory contact during inspections and audits and lead regulatory intelligence activities.

• Communicates and coordinates with VP and MTF senior management and other department heads on regulatory issues and regulatory strategies which may impact MTF's ability to fulfill its mission.

• Communicates with federal/state regulatory agencies, international government and notified bodies, and AATB related to applicable new or revised regulations and standards

• Assist on special projects and performs additional duties as assigned.

Qualifications

• Bachelor's degree in a scientific or related field, or a combination of education and equivalent work experience

• 7+ Years of overall experience

• 5 Years of Managerial experience

• 5 Years or Human tissue or medical device manufacturing

• Thorough understanding of FDA, QSR, cGMP, ISO regulations for medical devices, diagnostics or pharma Must exhibit people management, effective communication skills

• Attention to detail, critical thinking, problem-solving, and organizational skills

• Prior experience handling FDA inspections for medical devices, diagnostics, biologics and/or pharma Demonstrated success in obtaining US FDA regulatory clearance/approval for medical technologies

• Ability to travel up to 20% of time to MTF locations and to suppliers as required

Benefits Information

At MTF Biologics we provide comprehensive benefits and resources to support our employees physical, emotional, and financial health.

• 4 weeks Paid Time Off (PTO)

• Paid Holidays

• Medical, Dental, Vision Insurance and Prescription Drug Insurance

• 401K plan with company match

• Short & Long Term Disability

• Life & Accidental Death Insurance

• Tuition Reimbursement

• Health Care/Dependent Care Flexible Spending Accounts

• Adoption Assistance

• Voluntary Benefits (e.g., Pet Insurance, Legal, home and auto insurance)

• Sword Health (at home Physical Therapy)

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Job Location US-NJ-Edison

Type Full-Time

Category Regulatory Affairs

Shift Non-Shift (Standard Business Hours 8:15am-4:30pm EST)

Job ID 2026-7949