Role Description Our professional auditors are integral to our company's mission by ensuring the financial integrity of premium development. In this role, you will examine policyholders' operations and financial records to ensure exposures (such as payroll, sales, fixed assets) are accurately calculated within strict insurance guidelines and communicate audit findings through detailed formal reports. As a Premium Auditor, you will work out of your home, when not traveling to policyholders' locations. This position involves traveling to customer locations within a 50-mile radius of the Denver Colorado area. This position is eligible for mileage reimbursement. Open for experienced applicants. - Perform examination of policyholders' accounting and financial records to ensure accurate calculation of earned premium for smaller, less complex risks. - Ensure that audited exposures (payroll, sales, fixed assets, etc.) are accurately calculated within strict insurance guidelines. - Communicate audit findings through detailed formal reports supported by audit workpapers. - Review appropriate audit documentation and/or company policy systems, to determine specific coverages provided by the policy and plan audit strategy. - Investigate policyholder operations to obtain actual exposures, verify classifications as they apply to the policy and ensure conformity to various state laws and insurance regulations for the appropriate audit period. - Prepare detailed work papers and written correspondence in support of audit findings. - Identify issues to be communicated and socialize the audit information to appropriate stakeholders (i.e., Central Processing, Distribution, Underwriting, Agent/Broker, etc.) to elaborate on current risk conditions or initiate necessary changes to the policy contract. - With strict oversight, schedule audit appointments with policyholders taking into account priority of assignments and location within assigned territory. - Develop effective workload management skills through efficient time utilization including managing work-in-process and documenting progress for appropriate stakeholders/management. - Prepare routine administrative tasks such as: Time Tracking, Expense Reports, Mileage Reports, etc. Qualifications - Degree in Accounting preferred - Open for fresh graduates - Audit, compliance and finance experience is a big plus Benefits - Comprehensive benefits - Workplace flexibility - Professional development opportunities - Opportunities provided through Employee Resource Groups Company Description At Liberty Mutual, our goal is to create a workplace where everyone feels valued, supported, and can thrive. We build an environment that welcomes a wide range of perspectives and experiences, with inclusion embedded in every aspect of our culture and reflected in everyday interactions. This comes to life through comprehensive benefits, workplace flexibility, professional development opportunities, and a host of opportunities provided through our Employee Resource Groups. Each employee plays a role in creating our inclusive culture, which supports every individual to do their best work. Together, we cultivate a community where everyone can make a meaningful impact for our business, our customers, and the communities we serve. We value your hard work, integrity and commitment to make things better, and we put people first by offering you benefits that support your life and well-being. To learn more about our benefit offerings please visit: Liberty Mutual Benefits Liberty Mutual is an equal opportunity employer. We will not tolerate discrimination on the basis of race, color, national origin, sex, sexual orientation, gender identity, religion, age, disability, veteran's status, pregnancy, genetic information or on any basis prohibited by federal, state or local law.

Title: Senior Franchise Revenue Auditor - EMEAA (Remote) Location: United Kingdom Department: Audit and Risk Job Description: We’re looking for an experienced and driven Senior Franchise Auditor to join our Revenue Compliance & Audit team supporting franchise hotels across EMEAA. In this role, you’ll play a critical part in protecting brand integrity and financial accuracy by ensuring franchise hotels report revenues in line with Franchise License Agreements. You’ll lead revenue compliance audits end to end, partner closely with hotel leadership and internal stakeholders, and make well judged recommendations that drive transparency, consistency and continuous improvement. This is a fantastic opportunity for someone with a strong audit or finance background who enjoys working independently, building trusted relationships, and influencing outcomes in an international environment. What You’ll Be Doing • Plan and conduct revenue compliance audits for franchise hotels across EMEAA • Assess reported gross room revenues against Franchise License Agreements • Analyse data, identify exceptions, and clearly document audit findings • Communicate results to hotel General Managers and corporate stakeholders • Recommend corrective actions, negotiate settlements, and escalate potential risks or fraud where required • Contribute to ongoing improvement of audit methodologies, tools, and risk assessment approaches • Collaborate with Finance, Operations, and Franchise teams to resolve ambiguities and strengthen controls • Deliver agreed annual audit targets while maintaining high quality and accuracy standards Who We’re Looking For • Experience in internal audit, corporate accounting, or operations within the hospitality sector. • Strong understanding of hotel revenue reporting standards and processes • Confidence working with senior stakeholders, including Hotel General Managers • Excellent written and verbal communication skills in English • High attention to detail, strong analytical skills, and the ability to manage multiple priorities • Proficiency with Microsoft Office and exposure to hotel property management systems • Willingness to travel regionally as required (up to 40%) #LI-KW1 #LI-REMOTE

Title: Auditor, Medical Devices, Qualified 3rd Party Experienced - Full-Time Location: United States Job Description Experienced 3rd Party Qualified Medical Device Auditors - Full-time - Travel based Auditor. Interested in future career opportunities in the Quality Assurance audit and support services industry? We're looking for an experienced 3rd Party Qualified Medical Device Auditor that wants to build something great with an incredible group of people. By joining Intertek, your contributions will be valued as we continue to help the world Build Back Ever Better. Intertek's Business Assurance team goes beyond testing, inspection and certification to look at the underlying elements that make a company and its products successful. Our assurance solutions provide confidence and total peace of mind that a client's operating procedures, systems and people are functioning properly to provide a competitive advantage in the marketplace. What are we looking for? The Auditor, Medical Devices will support the Business Assurance business by leading and/or participating as an assessor during all phases of a client’s management system, in accordance with the company’s accredited certification program. The Auditor is the primary interface with the client before and during the process of all auditing activities. Additionally, the Auditor will help train low-graded Auditors through witness audits, technical support, and education of both client and sales force as needed. This will be a travel-based position, with extensive travel to client sites required. Candidate must be comfortable traveling 3 to 5 nights per week. This is a remote position; however, applicants must reside in and be able to legally work in the United States. Salary & Benefits Information Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. What you’ll do: - Audit client management systems for compliance with established standards, client, and/or industry requirements, government regulations, and other relevant standards, specifically ISO 13485, regulatory requirements for the US, Canada, Japan, Australia, and/or Brazil, and/or GMP regulatory requirements related to the medical device, pharmaceutical and/or cosmetic industry. - Assist clients with questions relevant to the audit and/or certification process. - Act as Lead Auditor or team member. - Travel will include overnight 3 to 5 days per week, to various worksites and client locations . - Coordinate audit activity with team members. - Liaison with client regarding audit activity. - Review client's quality management system documentation - Verify and document evidence of compliance and non-compliance. - Prepare audit report. - Review audit results with coordinator and other assessment team members. Make presentations to clients and/or certification board concerning audit results, when required. - Assist with corrective action requirements resulting from assessments. - Participate in audit meetings. - Review audit reports and provide technical assistance to the medical team. - Support management in areas of continuous improvement. - Provide management with updates on status of work, initiatives, and projects, as required. This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. Minimum Requirements & Qualifications: - 4 year college/university degree in a science or technical field (biology or microbiology; chemistry or biochemistry; computer and software technology; electrical, electronic, mechanical or bioengineering; human physiology; medicine; pharmacy; physics or biophysics) or equivalent combination of relevant education and work experience. - A minimum of 4+ years of full-time work experience in a 3rd Party Auditing with Lead Auditor qualification in MDSAP and ISO 13485:2016 with an up to date audit log - A minimum of 4+ years of full-time work experience in a medical device or related medical device industry (design, development, testing, quality assurance/quality control). - A minimum of 2+ years in a quality management systems environment (auditing, CAPA, complaints, management review) - Strong communication and interpersonal skills. - Sound judgment, organizational, and analytical skills. - Excellent computer and writing skills. - Ability to define problems, collect data, establish facts, and draw valid conclusions. - Ability to exercise effective time management skills in completion of assignments. - Must be willing and able to travel extensively. Primarily domestic travel, some international travel may be needed (typically includes USA+Canada+Mexico). - Possess a valid unrestricted driver’s license and the ability to operate a motor vehicle in the performance of the official duties of the position. Preferred Requirements & Qualifications: - Lead Auditor Training with (ISO19011 OR ISO13485) Certification - MDR Notified Body auditing experience - Related 3rd party auditing industry management systems experience with 3rd party audit log with 6 audits for a total at least 15 audit-days per 12-month period with at least 2 of these audits being initial or recertification audits and Lead Auditor role in at least 2 of these 6 audits within the last 12 months - Working knowledge of relevant regulatory requirements for medical devices and pharmaceuticals in the EU, US, Australia, Japan, Brazil, and/or Canada. - Experience implementing/auditing to ISO 13485, ISO 14971, and medical device regulatory requirements. - Device Industry experience with Orthopedic implants, Active devices, Software as a medical device, Monitoring devices, IVF and ART devices, and sterility requirements (ETO, GAMMA). - Specific experience/training on processes used in the relevant industry’s manufacturing (ex. sterilization, machinery, electric and electronic devices or components, software development). - Training/experience in quality tools (Kaizen, lean manufacturing, etc.). PHYSICAL REQUIREMENTS: This role requires the ability to: - Ascend or descend ladders, stairs, ramps, and the like, using feet and legs and/or hands and arms. Body agility is emphasized. - Stand, for sustained periods of time. - Walk, moving on foot to accomplish tasks and to move from one work location to another. - Communicate well, thru spoken word, conveying detailed accurate information & instructions to others. - Hear well, perceiving sounds with or without correction, including the ability to receive information thru oral communications. - Exert up to 10 pounds of force occasionally and/or negligible amounts of force frequently to lift, carry, push, pull or otherwise move objects. - Have close visual acuity to perform an activity such as preparing & analyzing data, viewing a computer monitor, reading, report writing, visual inspection, and use of measurement devises. Intertek: Total Quality. Assured. Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth. Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed. We Value Diversity Intertek’s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics. #LI-Remote #LI-JC1 *Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume. About Us Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life. About the Team The Business Assurance group of Intertek provides a full range of business process audit and support services, including management systems certification, sustainability and responsible sourcing audits, risk management, and training. Our range of bespoke auditing, performance benchmarking and supply chain solutions provide insight into every aspect of operations, allowing clients to make informed decisions about their business while ensuring their workforce competencies are current and relevant. Apply Now Job Info - Job Identification14636 - Job CategoryAUDITING - Job ScheduleFull time - Job ShiftFirst Shift - Locations 70 Codman Hill Road, Boxborough, MA, 01719, US - Regular or TemporaryRegular - Job TypeStandard - DepartmentBusiness Assurance -

Role Description The Clinical Trainer, EP will provide expert clinical product and technical assistance and training to physicians, EP Lab Staff, and country clinical specialists on the effective and safe use of our products during case procedures within SEA, and in a manner that leads to meeting and exceeding business goals. Key Responsibilities - Training - Develop training and development plan for new hires in respective countries. - Support cases (2D, 3D, Single Shot) with the newly trained team member and ensure that they support the clinical cases safely and professionally, and monitor their clinical competencies for products relating to respective market. - Identify learning needs of cath labs staff and conduct in-service session to improve their understanding in respective labs and countries. - Educate customers and internal BSC employees on the merits and proper clinical usage of our products by giving presentations and demonstrations to keep abreast with the latest product and technology developments for EP portfolio. - Partner with local teams to drive professional Education Program to Physicians where needed. - Organize, plan and conduct trainings for new product/software launches in respective sites for both internal and external customers to drive adoption and utilization. - Mentoring - Provide initial and continuous practical and in-field training to EP new hires and junior team members specialists on EP portfolio, development process, products and features, and procedures involving those products and features. - Follow up with new hires under your charge and track their progress in accordance with the development plan; and adjust it when necessary. - Identify learning gaps of mentees, and develop follow up action plans to bridge the gaps improve his/her clinical skills and knowledge. - Be the lead to ensure clinical excellence of the country team by providing guidance to clinical specialists as needed. - Clinical Case Support - Will be required to attend cases in labs of hospital accounts for case support and development efforts of our capital systems and their components. - Respond to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel to develop optimal solutions. - Serve as primary contact point for clinical support and arrangement in the areas of case coverage, troubleshooting for EP systems and catheters, in the ASEAN region, to ensure the franchise clinical excellence. - Self-Improvement - Keep abreast with updated publications relating to key aspects of BSC product and technology, in particular PFA and Rhythmia. - Maintain advanced clinical knowledge of cardiac ablation, cardiac ablation components, technical knowledge of EP technology, advancements, and changing EP landscape. - Embark on enrichment programs to upskill oneself to enhance personal performance. Company Description Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn .