Regulatory Affairs Specialist Kelly Services - 3.8 Goose Creek, SC Job Details Full-time $70,000 - $120,000 a year 3 hours ago Benefits Paid holidays Disability insurance Health insurance Dental insurance Vision insurance Retirement plan Paid sick time Qualifications Customer complaint resolution Full Job Description Medical Device Industry Kelly Science is seeking an experienced Regulatory Affairs Specialist to support regulatory strategy, submissions, and ongoing compliance for a medical device organization. This position is ideal for a hands-on regulatory professional with 5-10+ years of experience who understands the requirements for bringing Class II and/or Class III medical devices to market and maintaining regulatory compliance throughout the product lifecycle. Key Responsibilities Support regulatory strategy and pathway development for new and existing medical devices. Prepare, coordinate, and maintain regulatory submissions and supporting documentation for FDA and other applicable regulatory authorities. Support FDA submissions and regulatory activities associated with Class II and Class III medical devices . Serve as a regulatory subject matter resource for cross-functional teams throughout product development, validation, manufacturing, and commercialization. Ensure products and associated documentation comply with applicable FDA regulations and quality system requirements. Maintain knowledge of 21 CFR Part 820, ISO 13485, ISO 9001 , and other applicable standards and regulatory requirements. Monitor changes to regulations, standards, and FDA guidance and communicate potential impacts to internal stakeholders. Support regulatory documentation, technical files, dossiers, change assessments, and product lifecycle activities. Partner with Quality, Engineering, Manufacturing, Operations, and other functions to ensure regulatory requirements are incorporated into projects and product changes. Review product and process changes for potential regulatory impact and determine appropriate documentation or submission requirements. Support internal, customer, supplier, and regulatory audits as needed. Assist with CAPA, complaint investigations, document control, supplier quality, and other Quality System activities where regulatory expertise is required. Review and support IQ/OQ/PQ and validation documentation for regulatory and Quality System compliance. Support risk-management activities, including FMEA and related product/process documentation. Maintain accurate, inspection-ready regulatory records and documentation. Communicate with regulatory agencies as appropriate and assist with responses to agency questions and requests. Perform other regulatory and quality-related duties as assigned. Qualifications 5-10+ years of relevant Regulatory Affairs experience , preferably within the medical device industry. Demonstrated experience with FDA-regulated medical devices and applicable U.S. regulatory requirements. Experience with Class II and/or Class III medical devices strongly preferred. Working knowledge of 21 CFR Part 820, FDA Quality System requirements, ISO 13485, and

ISO 9001

. Experience preparing or supporting medical device regulatory submissions and associated technical documentation. Understanding of medical device product development, manufacturing, validation, and commercialization processes. Experience working within an established Quality Management System. Ability to interpret regulatory requirements and translate them into practical requirements for cross-functional teams. Strong technical writing, documentation, organization, and project-management skills. Excellent written and verbal communication skills with the ability to work effectively across Quality, Engineering, Manufacturing, and business teams. Strong attention to detail and ability to manage multiple regulatory priorities and deadlines. Education Bachelor's degree in Engineering, Life Sciences, Biomedical Sciences, Regulatory Affairs, or a related technical discipline required. Advanced degree or relevant regulatory/quality certifications are a plus. Preferred Experience Candidates with experience in one or more of the following areas are especially encouraged to apply: FDA medical device submissions Class II and Class III devices

ISO 13485

Quality Management Systems Design controls and risk management IQ/OQ/PQ and process validation CAPA and complaint handling Internal or regulatory audits Supplier quality Regulatory change assessments Technical documentation and regulatory dossiers Kelly Science connects experienced scientific, engineering, quality, and regulatory professionals with opportunities where their expertise can make an impact. We are looking for a regulatory professional who can work independently, collaborate across functions, and help ensure medical devices meet applicable regulatory requirements from development through commercialization. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Why Kelly® Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.