About this opportunity
Musculoskeletal Transplant Foundation lists this Manager, Regulatory Affairs opportunity in edison, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
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 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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Worksite address
edison, NJ, 08818, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.