Supv., Asuntos Regulatorios y Aseguramiento de

Are you looking for a company that cares about people’s lives and health, including yours? At Olympus, we help make people’s lives healthier, safer and more fulfilling, every day.**_Let’s inspire healthier lives, together._**This position is responsible for overseeing local regulatory and quality system activities for Mexico. This function prepares final registration dossiers for submission to the Mexican regulatory agency (COFEPRIS) and acts as a liaison between Olympus Mexico (OMS) and COFEPRIS. As part of this function, this individual also acts as the Sanitary responsible representative for OMS and also as QA Management Representative and responsible for the QMS at OMS. Thus, responsible for ensuring that OMS and 3rd party vendors working on behalf of OMS comply with all applicable quality, regulatory and legal requirements in Mexico. This function is responsible for ensuring the identity and safety of the products is maintained at any facility where Olympus product is serviced, stored, or distributed in Mexico. This function supports the procurement, organization, logging and filing of regulatory documentation related to product registrations and vigilance activities in Mexico. This function will also be responsible to support regional activities/projects.**Job Duties**:**Job Requirements**:**Education / Training**:Bachelor’s Degree in science, biology, chemistry or a related field compatible with the requirements for a Sanitary Responsible representative in Mexico Certificate / License / Registration ISO 13485 preferred. Knowledge of business and management principles, including performance management Solid knowledge of Mexico regulatory processes, including class II & III medical devices.**Experience**: Minimum 5 years direct experience in regulatory affairs and quality assurance at a medical devices or pharmaceutical company. Experience working with COFEPRIS, registering class II & III medical device. Experience working in quality management systems such as ISO 13485 or equivalent. Experience in all aspects of Quality Assurance (QSR, ISO 13485, MDSAP, complaint handing, ISO assessments, risk management, etc.) **Skills**:Strong organizational skills with ability to prioritize workload. Must be detail-oriented, self-motivated, and able to work independently in a multi-tasking environment. Must have strong presentation and communications skills in both Spanish and English. Must have the ability to work under pressure within time critical deadlines. Strong general computer skills.**_ We realize work isn’t just a job to you._**It’s a big part of your life, but not the only part. That’s why we offer competitive salaries, annual bonus program and comprehensive medical benefits, as well as tuition reimbursement, flexible schedules, parental and adoption leave, on-site services and Colleague Affinity Networks — so you can be ready for where life can take you.Olympus is a global technology leader, crafting innovative optical and digital solutions in medical technologies; life sciences; industrial solutions; and cameras and audio products. Throughout our 100-year history, Olympus has focused on being true to society and making people’s lives healthier, safer and more fulfilling.**Olympus True To You. True To Society. True To LIFE.**Olympus embraces diversity and inclusion. As an Equal Opportunity Employer, our policies as well as our values prohibit unlawful discrimination based on an employee's or applicant's race, color, sex, age, physical or mental disability, national origin, religion, sexual orientation, gender identity and/or expression, marital status, genetic information, ancestry, military or veteran status, or any other federal, state or local protected classification. EOE Minorities/Females/Veterans/DisabledPosting Notes: || Mexico (MX) || Ciudad de México (MX-CMX) || Mexico, D.F. ||