• Manage and publish daily content across Facebook, Instagram, and other active platforms • Develop and maintain a monthly content calendar in coordination with the team lead • Write captions and short-form copy tailored to a professional dental audience (B2B and B2C) • Monitor comments, DMs, and community interactions — respond or escalate within 24 hours • Manage and moderate the company's Study Club Facebook Group, a community for dental professionals to share clinical cases • Set up, manage, and optimize paid campaigns on Meta Ads Manager: awareness, lead generation, and retargeting • Build audience segments using custom audiences, lookalikes, and interest-based targeting • Monitor daily ad spend and performance; make real-time adjustments to stay within budget and hit targets • Run A/B tests on creative, copy, and audience targeting; document and apply learnings • Produce monthly performance reports: CPL, CTR, ROAS, reach, and frequency with recommendations • Coordinate with the designer on ad creative briefs and required asset specs • Edit testimonial and product videos from raw footage (up to 3 hours of footage per project) • Add subtitles, lower thirds, motion graphics, and branded end cards per brand guidelines • Export platform-optimized versions for Facebook, Instagram Reels, and YouTube • Ensure consistent brand tone and visual style across all video outputs • Monitor website traffic via Google Analytics (GA4); flag notable changes in traffic sources or behavior • Track UTM parameters and campaign links to ensure accurate source attribution • Conduct basic keyword research to inform social content and web copy needs • Support landing page performance monitoring and surface optimization suggestions • Assist with scheduling and deploying email campaigns through Mailchimp • Maintain and update email lists — segmentation by region, specialty, and engagement status • Ensure list hygiene: process unsubscribes, bounces, and re-engagement flags regularly • Compile leads from paid and organic channels daily; organize by source, date, and quality • Send a structured morning lead report to the U.S. sales team by 9:00 AM EST each business day • Flag high-priority leads for immediate follow-up by the sales team • Maintain lead attribution tagging for monthly reporting and campaign ROI tracking • Maintain billing and vendor invoice tracking in Excel or Google Sheets — log payments, due dates, and approvals • Update campaign tracking spreadsheets: ad budgets, spend actuals, and performance summaries • Maintain shared digital asset folders and campaign documentation for team reference • Support platform account management: ad account settings, pixel setup, and audience updates

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Regulatory Affairs Group Job Sub Function: Regulatory Affairs Job Category: Professional All Job Posting Locations: Danvers, Massachusetts, United States of America, Remote (US) Job Description: About Cardiovascular Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Weare searching for the best talent for a Manager, Regulatory Affairs to support Digital Health in our Heart Recovery business. The preferred location for this role is within a commutable distance of Danvers, MA however remote options within the United States will be considered on a case-by-case basis and if approved by the company. Purpose: The Regulatory Affairs Manager, Digital Health, in partnership with the Director, RA Digital Health and the RA team, will be responsible for developing and executing strategies to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to existing devices. In addition, this role will serve as a liaison for our global regulatory teams as we expand our product approvals across geographies. You will partner with global teams to inform regulatory requirements as a key member of cross-functional teams, prepare and review FDA submissions, and interact with and respond to FDA pre-submission during the review period. You will support global regulatory teams as an interface with the product development teams in Digital Health. Your core focus will be regulatory leadership for Digital Health across Heart Recovery’s cardio-pulmonary product portfolio: the Impella Ecosystem (Heart Pumps), PreCardia (cardio-renal unloading - decompensated heart failure (ADHF), restoring kidney function) and Breethe (ECMO: respiratory failure) with particular emphasis on: - Cybersecurity & Interoperability - Software (SiMD and SaMD and AI/ML based clinical decision support) - Systems Engineering and liaison with the Clinical/Medical office as needed to establish robust V&V of the product portfolio. - Digital Health Policy and Intelligence to ensure that global regulations are considered in product development and design Through your engagement in this role, you will help shape the life-saving field of Heart Recovery. You will be responsible for: - Independently support cross-functional new product development projects with a specific focus on cybersecurity, software (SiMD and SaMD and AI/ML based clinical decision support), and hardware aspects, and lead compilation of all materials required for submissions to FDA. - Provide ongoing support to project teams for regulatory issues and questions. Find, interpret, and apply global digital health regulations and guidance appropriately for situations. - Provide regulatory support for currently marketed products as necessary to ensure ongoing compliance. - Provide support for changes to existing products, including providing regulatory assessment of changes and subsequent regulatory filings. - Develop solutions to a variety of technical problems. Actively participate in problem solving discussions and recommend solutions. - Keep abreast of global Digital Health guidance documents and regulations and monitor impact of changing regulations on submission strategies. - Assist in the maintenance and improvement of digital health regulatory SOPs. - Interact and negotiate with regulatory agencies on defined matters as needed. - Have Regulatory Affairs experience in the medical device industry with a track record of successful FDA submissions that include cybersecurity (524B compliance), software and hardware components . - Be passionate about Regulatory Affairs impact in support of the research, development, clinical, marketing, and production of state-of-the-art class III cardiovascular medical devices. - Be energized by joining a world-class company and regulatory team. - Enjoy teamwork and thrive as a member of dynamic cross-functional teams. - Build and maintain strong interpersonal relationships within and outside of the company. - Exhibit leadership traits: positive, forward looking, accountable, action-oriented, delivering results. - Be adaptable and thrive in a dynamic work environment where variety is the routine. - Embrace change, continuous learning, and work skills improvement. Qualifications / Requirements: - Minimum of a Bachelor’s Degree is required, Advanced degree strongly preferred; Computer Science/Engineering discipline highly desired. - At least 6+ years Regulatory Affairs experience (5+ with Advanced Degree) in the medical device space is required; experience with complex networked device ecosystems like Cardiac Electrophysiology, Diabetes, Neuromodulation, Robotic Surgery etc. strongly preferred. - Regulatory Affairs experience in the medical device industry with a track record of successful FDA submissions or FDA review experience in Cybersecurity (524B), SiMD and SaMD required. - History of successful IDE/PMA/510(k) device submissions (Class III device submissions preferred) that include hardware and software components required. - Experience independently communicating with FDA reviewers and leading Q-sub meetings and informal discussions with reviewers required. - Experience supporting software device development (for example SiMD, SaMD, Cybersecurity, IEC 62304/82304 etc). - Experience with FDA requirements, guidance documents, ISO 14971, ISO 13485, IEC 60601, IEC 62304, Cybersecurity 524B compliance, interoperability. - Experience in reviews of engineering, manufacturing, marketing, labeling and clinical documents for regulatory compliance. - Ability to effectively manage multiple projects and priorities. - Strong communication and regulatory writing skills. - Strong problem-solving skills, interpersonal skills, and effective team member. - Results oriented. Ability to drive to completion in adherence to aggressive project schedules. - Ability to comprehend principles of engineering, physiology and medical device use. - Class III cardiovascular device experience strongly preferred. - Regulatory Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society) preferred. - AI/ML and/or PCCP experience is a plus. - Travel up to 10% Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource. #LI-Remote Required Skills: Preferred Skills: Analytical Reasoning, Business Writing, Coaching, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Risk Compliance, Strategic Thinking, Technical Credibility The anticipated base pay range for this position is : $117,000.00 - $201,250.00 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

ABOUT US: CEF Solutions Inc. is a Consulting Services and Business Process Outsourcing (BPO) company specializing in BPO Operations, Operations Management, Process Engineering and Innovation, Cost Optimization, and Staffing solutions. We take pride in our expertise in providing specialized staffing services, ensuring that clients have access to top talent that aligns with their operational goals. We service some of the largest multinational companies in the world and are expanding quickly by delivering an unmatched end-to-end client experience. Company website: www.CEF.inc JOB DESCRIPTION: We are looking for a well-rounded Digital Marketing & Social Media Specialist with 3–5 years of experience to join our remote Marketing Communications team. This role covers social media management, paid advertising, video editing, performance reporting, and day-to-day digital marketing operations. The right person is equally comfortable running a Meta ad campaign, editing a testimonial video, and keeping tracking spreadsheets clean and up to date. Responsibilities Social Media Management - Manage and publish daily content across Facebook, Instagram, and other active platforms - Develop and maintain a monthly content calendar in coordination with the team lead - Write captions and short-form copy tailored to a professional dental audience (B2B and B2C) - Monitor comments, DMs, and community interactions — respond or escalate within 24 hours - Manage and moderate the company's Study Club Facebook Group, a community for dental professionals to share clinical cases - Conduct basic social listening: track competitor activity and identify outreach or content opportunities Paid Advertising — Meta Ads - Set up, manage, and optimize paid campaigns on Meta Ads Manager: awareness, lead generation, and retargeting - Build audience segments using custom audiences, lookalikes, and interest-based targeting - Monitor daily ad spend and performance; make real-time adjustments to stay within budget and hit targets - Run A/B tests on creative, copy, and audience targeting; document and apply learnings - Produce monthly performance reports: CPL, CTR, ROAS, reach, and frequency with recommendations - Coordinate with the designer on ad creative briefs and required asset specs Video Editing - Edit testimonial and product videos from raw footage (up to 3 hours of footage per project) - Add subtitles, lower thirds, motion graphics, and branded end cards per brand guidelines - Export platform-optimized versions for Facebook, Instagram Reels, and YouTube - Ensure consistent brand tone and visual style across all video outputs - Manage video file organization and maintain a library of finished and raw assets SEO & Content Performance - Monitor website traffic via Google Analytics (GA4); flag notable changes in traffic sources or behavior - Track UTM parameters and campaign links to ensure accurate source attribution - Conduct basic keyword research to inform social content and web copy needs - Support landing page performance monitoring and surface optimization suggestions Email Marketing Support - Assist with scheduling and deploying email campaigns through Mailchimp - Maintain and update email lists — segmentation by region, specialty, and engagement status - Ensure list hygiene: process unsubscribes, bounces, and re-engagement flags regularly - Pull post-send performance reports: open rate, click rate, unsubscribe rate, and list growth Lead Management - Compile leads from paid and organic channels daily; organize by source, date, and quality - Send a structured morning lead report to the U.S. sales team by 9:00 AM EST each business day - Flag high-priority leads for immediate follow-up by the sales team - Maintain lead attribution tagging for monthly reporting and campaign ROI tracking Marketing Admin & Operations - Maintain billing and vendor invoice tracking in Excel or Google Sheets — log payments, due dates, and approvals - Update campaign tracking spreadsheets: ad budgets, spend actuals, and performance summaries - Maintain shared digital asset folders and campaign documentation for team reference - Support platform account management: ad account settings, pixel setup, and audience updates Requirements - 3–5 years of experience in digital marketing, social media, or a related role - Proven hands-on experience with Meta Ads Manager — campaign setup, optimization, and reporting - Video editing experience with Adobe Premiere Pro, CapCut, or equivalent tools - Comfortable writing professional English copy for social media and marketing communications - Solid working knowledge of Google Analytics (GA4) and UTM tracking - Strong Excel or Google Sheets skills — organized reporting and basic formulas expected - Able to work with EST overlap for daily lead reporting and team check-ins - Detail-oriented and comfortable managing multiple workstreams independently Nice to Have - Experience with Mailchimp or other email marketing platforms - Familiarity with social listening tools (Sprout Social, Mention, or similar) - Motion graphics or After Effects experience - Background in healthcare, dental, or B2B professional audience marketing

• Daily reporting and monitoring of campaigns to ensure performance goals and revenue objectives are met while managing an ever-growing amount of campaigns. • Liaise with partners and sales reps, building long term relationships and making custom deals. • Analyze data and update the team on hot opportunities and market trends. • Brainstorming with media managers and other colleagues to improve processes. • Launch new international campaigns every day. • Stay up-to-date on industry trends. • Manage large monthly budgets.