Role Description The Pharmacovigilance Analyst will support the Local Pharmacovigilance Organization in several LPV operations and compliance tasks related to the vigilance of the Kenvue product portfolio under the umbrella of the Local Safety Officers (LSOs). The Pharmacovigilance Analyst will work in close partnership with the LPVEx group, Regional Heads and Local Safety Teams to centralize activities to ensure consistent operations approach across the regions in alignment with the LPV processes for areas of responsibility, enabling process optimization and increasing efficiency. You will collaborate with cross-functional teams to ensure patient safety and product efficacy: - Support the LSOs on applicable operational tasks and coordinate communications to the LPV Organization. - Work in close partnership with members of LPV across all regions to ensure a global consistent approach for Safety. - Manage the Group Mailbox and LPV SharePoint site. - Oversee timely delivery of the requested Pharmacovigilance System Master File (PSMF) annexes per PV regions. - Key contributor for the Annex A (Contact details for Local PV Contacts Nominated at National Level) & C (Company Units responsible for safety data collection of solicited and spontaneous cases). - Ensure appropriate Quality checks being performed in accordance with PSMF Policies. - Maintenance/generation of AE/PQC contact list for PVA contracts, LSO contact list and Art 57 lists to ensure accurate information is shared with others. - Manage LPV members information (new hires, termination, etc.) on global data base. - Manage assignment of trainings per role, access to SharePoint and support addition on Distribution List, in close cooperation with Regional LPV Teams. - Support Local Pharmacovigilance Organization on the translation of regulatory requirement to reporting rules on the safety system. - Support on Investigations and CAPAs for LPV. Qualifications - Computer literate with knowledge of safety database systems, including reporting rules management and report generation. - Fluent communication skills in English, any additional language is a plus. - Qualification in Medical/ Health Sciences and/or proven equivalent experience in pharmacovigilance and/or data management. - Excellent social, organizational, oral, and written communication & presentation skills. - Detail-oriented & compliance mindset skills. - Efficient, flexible, and dynamic team player. - Able to work effectively with different cultures and instill a culture of diversity and inclusion. Requirements - Experience with AI-driven pharmacovigilance platforms. - Demonstrated ability to innovate within R&D environments using cutting-edge analytical methods. - Exceptional skills in interdisciplinary collaboration bridging scientific research with computational tools. - Passion for pioneering new solutions for operational activities. Company Description Kenvue is currently recruiting for a Pharmacovigilance Analyst. At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you!

Role Description Due to growth, we are looking for two Medical Information Supervisors to join our global Medical Information team at ProPharma. Based in the Philippines, you will be responsible for a US based team of Medical Information Specialists. This is a fully remote role and the working hours are in line with our American colleagues. Please note: Working hours will be US working hours/EST. The role is Monday - Friday (40 hours). The Medical Information Supervisor is responsible for providing an excellent quality and efficient Medical Information (MI) service in respect of designated clients/products, including intake and documentation of Medical Information, product complaint and adverse event cases. Main Responsibilities - Medical Information service delivery: - Providing an excellent quality and efficient medical information enquiry handling service by answering technical questions in respect of designated products in an accurate, confident, and professional manner. - Being knowledgeable and complying with the specific Working Practices (WPs) which have been agreed with designated clients. - Independently ensuring that tasks are completed within the deadlines and Key Performance Indicators (KPIs) documented in the agreed ProPharma Standard Operating Procedures (SOPs) and WPs. - Supporting junior members of the team in ensuring that their tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs as requested by Management. - Recognizing adverse events and defective product reports and handling and reporting these in strict compliance with agreed ProPharma SOPs and WPs. - Able to communicate effectively with the Company’s clients as appropriate. - Maintaining awareness of, and ensuring compliance with, the legal requirements and professional guidelines associated with the provision of medical information on behalf of the Pharmaceutical Industry. - Identifying where company-specific WPs/Client Instructions may require updating. - Workload Management: - Taking responsibility for assessing current workload status of team members and ensuring the fair distribution of workload. - Able to redistribute workload to ensure all deadlines are met. - Able to maintain an oversight of the team’s performance against the agreed KPIs, feeding back to management and the team on improvements needed or providing positive feedback as required. - Able to plan ahead to organize workload to take into account Public Holiday periods including annual leave and ad hoc cover as applicable. - Motivating the team to provide an efficient and effective Medical Information service. - Quality Assurance: - Consistently maintaining quality in all areas of the job, particularly reporting of Adverse Events (AEs), Product Quality Complaints (PQCs) and logging enquiries into the Enquiry Handling System. - Performing quality checks on AEs, PQCs and correspondence to ensure accuracy in all areas of the job for other team members and providing training feedback. - Other quality tasks which may include checking client communications, weekly reports, new starter training paperwork and investigating complaints and deviations. - Training: - Supporting the induction and training of new members of staff. - Supporting and coaching other team members to ensure ProPharma’s processes are followed. - Providing accurate guidance on professional and technical questions, including support on non-standard enquiries. - Taking responsibility as required for identifying and coordinating future training needs for the team (ProPharma and client). - Involvement in some significant training sessions as requested by management. - Identifying areas to improve in relation to existing training sessions, or new training sessions which may be required by the team. - Supporting the overall business: - Developing and improving processes, including updating any necessary documentation, training staff, and communicating updates to relevant people. - Taking responsibility as required for leading a significant project(s) within the team(s). - Coordinating, planning, and training out of the project and ensuring regular status updates are provided to management. - Taking responsibility as required for being point of contact for designated clients. - Responding to client emails in a timely manner with minimal changes required to the email content by Manager. - Leading client meetings, taking action minutes and following up on actions. - Addressing client questions on case management and processes. - General: - Having an excellent working knowledge of, and to comply with, the SOPs of ProPharma. - Complying with the Company’s health and safety policies. - Ensuring the Confidentiality Statement within the Contract of Employment is always adhered to. - Proactively communicating feedback areas for the team and the individual to develop and improve in catch ups with Manager. - Ensuring that any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations. - Acting as a role model to other members of staff, acting in a positive and professional manner always. Qualifications - Excellent knowledge of medical information services and healthcare provision systems in the designated country. - Sound understanding of the pharmaceutical industry. - Able to understand, analyze and communicate pharmacological and medical issues concerning a broad range of pharmaceutical products. - Able to work within a team in a positive, open and professional manner at all times. - Able to motivate the team and encourage them to work efficiently. - Self-motivated to maintain high efficiency and productivity levels. - Excellent written and oral communication skills and computer literacy. - Excellent planning, prioritizing and organizational skills. - Able to coordinate and prioritize a team’s workload efficiently. - Able to project and maintain professionalism in handling difficult situations. - Strong decision making and problem-solving skills. - Able to identify potential process improvements. - Able to occasionally work extended and/or flexible schedule to meet client requirements. Requirements - Track record of success as a pharmaceutical Medical Information Professional, with at least 18 months prior Medical Information experience or equivalent. - A degree in a life science or pharmacy or equivalent. Benefits - We celebrate our differences and strive to create a workplace where each person can be their authentic self. - We are committed to diversity, equity, and inclusion. - Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. - With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

Role Description The Clinical Application Specialist CEE (exc. Poland) for Indirect Market, Image Guided Therapy Devices (IGT-D) at Philips is responsible for delivering exceptional clinical and product expertise to support business growth through indirect channels. This role focuses on equipping distributors, partners, and their customer base with the knowledge and tools needed to effectively utilize Philips’ industry-leading physiology and intravascular imaging solutions for coronary, cardiac solutions and peripheral applications in Central and Eastern Europe. - Provide advanced clinical education and training to distributor teams and end-users, including pre-sales presentations, product demonstrations, and hands-on application training sessions. - Support partners in assessing customer needs and tailoring Philips product solutions through detailed clinical specifications and workflow optimization recommendations. - Assist with the development and delivery of training programs for hospital staff, ensuring optimal use of Philips IGT-D technology in clinical environments. - Act as a resource for distributors and customers by offering expertise on product features, clinical applications, and troubleshooting, thus enhancing product adoption and utilization. - Collaborate with sales, marketing, and internal stakeholder groups to provide market intelligence and feedback on competitive activity and opportunities for product enhancements. - Develop and nurture strong relationships with partner organizations and end-customers, including physicians, cath lab staff, and business office personnel. - Contribute to achieving disposable product revenue targets in assigned territories by supporting indirect channel activities and strategic initiatives. - Serve as the main point of contact for customer inquiries and support when sales managers or distributor representatives are unavailable. - Collaboration with international teams and departments. Qualifications - Bachelor’s degree or higher in a relevant clinical or scientific field (e.g., biomedical engineering, nursing, medical technology). - At least 3 years of experience as a Clinical Application Specialist. - Experience in interventional cardiology, vascular surgery product group or similar is highly preferred. - Proven experience in clinical applications, medical devices, or healthcare technology, preferably with indirect market exposure. - Excellent communication and presentation skills, with the ability to educate and influence diverse stakeholders. - Strong organizational and problem-solving abilities, with a customer-centric approach. - Proficiency in MS Office (Word, Excel, PowerPoint) and ability to work effectively with digital tools. - Ability to travel within assigned territories as required. - Willing to travel extensively. - English proficiency is a must; other CEE language is a plus. How we work together We believe that we are better together than apart. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. Company Description We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. - Learn more about our business. - Discover our rich and exciting history. - Learn more about our purpose.

Job DetailsJob Location: Remote, TN - Franklin, TN 37067Position Type: Full TimeEducation Level: High School Diploma/GEDJob Category: Other PositionsUS Heart and Vascular is looking for a Remote Cardiac Monitor Specialist to join our team. $3000.00 Sign-on Bonus Available. Position Summary Monitors patients with implanted cardiac devices, including pacemakers, defibrillators, and remote monitoring systems. Analyzes device data, providing technical support to patients and healthcare providers, and ensuring optimal device performance and patient care from a remote setting. Responsibilities: Remotely monitors patients' cardiac devices, including pacemakers, defibrillators, and other implantable cardiac devices, to track device performance, patient data, and any abnormal findings. Reviews and analyzes device data, including ECGs, event logs, and diagnostic reports, to assess device function and identify any issues or potential complications. Provides technical support and education to patients regarding their cardiac devices, including troubleshooting issues, answering questions, and guiding patients on device usage and maintenance. Works closely with cardiologists, electrophysiologists, and other healthcare professionals to communicate findings, provides updates on patient status, and coordinate care as needed. Responds to alerts and notifications from cardiac devices regarding patient conditions, such as arrhythmia or device malfunctions, and takes appropriate action. Maintains accurate and detailed records of patient interactions, device data, and any relevant observations. Ensures that all documentation is complete and up-to-date in the electronic health record (EHR) system. Ensures that all activities and procedures comply with relevant regulations, standards, and best practices related to cardiac device management and remote monitoring. Requirements: Knowledge and understanding of cardiac devices and clinical or remote patient monitoring practices. Strong understanding of cardiac device technology, including pacemakers, defibrillators, and remote monitoring systems. Excellent analytical skills and the ability to interpret complex device data and ECGs. Exceptional communication skills, with the ability to provide clear instructions and support to patients and healthcare providers remotely. Proficiency in using remote monitoring software, electronic health record (EHR) systems, and other relevant technology. Ability to work independently and manage time effectively in a remote work environment. A bachelor’s degree in nursing, Cardiovascular Technology, Biomedical Engineering, or a related field. Two (2) years of experience in monitoring, calibrating, or maintaining cardiac devices is required Certification in cardiac device management or similar certification (e.g., CCDS, RCIS) is preferred. Qualifications