Manager, Regulatory Affairs

MTF Biologics; Edison (NJ); On-site; USD 99,000 - 125,000; Full time

Benefits offered by this job

4 weeks Paid Time Off (PTO)

401K plan with company match

Medical, Dental, Vision Insurance

Tuition Reimbursement

Job summary

MTF Biologics, located in Edison, New Jersey, is seeking a Regulatory Affairs Manager to oversee regulatory functions and ensure compliance with U.S. and international regulations. Responsibilities include leading a team, managing submissions, and developing regulatory strategies for new products.

The ideal candidate will have over 7 years of experience in regulatory affairs, with a bachelor's degree in a scientific field and proven managerial skills. The role offers a competitive salary with a comprehensive benefits package, including paid time off and health insurance.

Qualifications

• 7+ years of overall experience.
• 5+ years of managerial experience.
• 5+ years in human tissue or medical device manufacturing.
• Thorough understanding of ISO regulations.

Responsibilities

• Lead and develop Regulatory Affairs staff.
• Assist in managing the budget for the department.
• Oversee regulatory submissions for U.S. and international markets.
• Ensure maintenance of applicable licenses and certifications.
• Communicate with regulatory agencies on standards and regulations.

Skills

FDA regulations

People management

Communication skills

Problem-solving

Attention to detail

Education

Bachelor's degree in a scientific or related field

Job description

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

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)