Regulatory Specialist Ii
hace 3 semanas
**SUMMARY OF DUTIES**This position is responsible for coordinating and preparing regulatory submissions on a global level for the United States, Europe and other international countries. Other responsibilities include coordinating recalls, assisting with FDA facility inspections, Notified Body audits, and assisting with MDR, MPR, or Vigilance report recommendations.**ESSENTIAL FUNCTIONS PERFORMED**- Assist with determining global regulatory pathways for various projects including product classification and type of regulatory submission or rationale required.- Participates on various teams to define regulatory requirements of U.S. and international submissions, Technical Files or regulatory rationales.- Identifies guidance documents, international standards, Consensus Standards and assists teams with their interpretation.- Prepares regulatory submissions to the FDA, the Notified Body and other Ministries of Health.- Interacts with various levels of management, external agencies and companies.- Assist with analysis and making recommendations regarding complaints received by Merit Medical and whether they are MDR, MPR, or Vigilance reportable; participates in complaint related meetings.- Assist with developing, maintaining and analyzing department systems and provides training when needed.- Participates in and assists with FDA facility inspections, Notified Body Audits and other governmental inspections as directed.- Performs other related duties and tasks, as required.**SUMMARY OF MINIMUM QUALIFICATIONS**- Education and/or experience equivalent to a Bachelor's Degree in the biological, physical, engineering or material science disciplines and four years of related experience.- Knowledge of U.S. FDA regulations, the Medical Devices Directive (93/42/EEC, as amended), and ISO 13485 Quality System Standards.- Supervisory skills are preferred.- Self-motivated, self-directing, strong attention to detail and excellent time management skills.- Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.- Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.**COMPETENCIES**- Regulatory submission/rationale preparation- Assistance with medical device and vigilance reporting- Computer skills/internet research- Interpersonal/communication skills- Assistance with regulatory system development/trainingMERIT MEDICAL SYSTEMS, INC.EQUAL OPPORTUNITY EMPLOYER M/F/D/VLI-MM1**Requirements**:At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.As an eligible Merit employee, you can expect the following:- **Multiple Shifts and Hours** to choose from**:Days, Swing (Eve), and Nights**:- **Medical/Dental & Other Insurances** (eligible the first of month after 30 days)**3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays**- **401K | Health Savings Account****Follow Us**:**Day in the Life**:
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Tijuana, México Medtronic A tiempo completoA global healthcare technology leader is seeking a Senior Regulatory Affairs Specialist in Tijuana, Mexico. The role involves assessing device changes for regulatory implications, developing global strategies, and working closely with teams to ensure compliance with regulations. Candidates must have at least a Bachelor's degree and 4 years of relevant...
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Tijuana, México Medtronic A tiempo completoA global healthcare technology leader is seeking a Senior Regulatory Affairs Specialist in Tijuana, Mexico. The role involves assessing device changes for regulatory implications, developing global strategies, and working closely with teams to ensure compliance with regulations. Candidates must have at least a Bachelor's degree and 4 years of relevant...
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Regulatory Affairs Specialist
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Senior Regulatory Affairs Specialist
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Tijuana, México Merit Medical Systems Inc. A tiempo completoWhy Merit?En Merit Medical, nuestra misión es desarrollar dispositivos médicos innovadores que mejoren vidas. Nuestro objetivo es integrar y desarrollar a gente que quiere construir a través de trabajo duro, en equipo y comprometido, dispositivos que salvan vidas. Juntos estamos haciendo la diferencia en la vida de pacientes de todo el mundo.ESSENTIAL...
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Senior Regulatory Affairs Specialist
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Tijuana, México Merit Medical Systems Inc. A tiempo completoWhy Merit? En Merit Medical, nuestra misión es desarrollar dispositivos médicos innovadores que mejoren vidas. Nuestro objetivo es integrar y desarrollar a gente que quiere construir a través de trabajo duro, en equipo y comprometido, dispositivos que salvan vidas. Juntos estamos haciendo la diferencia en la vida de pacientes de todo el mundo. ESSENTIAL...
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Trade Compliance Analyst II — Import/Export Operations
hace 4 semanas
Tijuana, México Merit Medical Systems A tiempo completoA leading medical device company in Tijuana is looking for a Trade Compliance Analyst II to coordinate import/export documentation, ensure regulatory compliance, and provide excellent customer service. This role requires 5 years of experience and strong organizational skills. Responsibilities include preparing documents, reviewing shipping documentation, and...
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Trade Compliance Analyst II — Import/Export Operations
hace 4 semanas
Tijuana, México Merit Medical Systems A tiempo completoA leading medical device company in Tijuana is looking for a Trade Compliance Analyst II to coordinate import/export documentation, ensure regulatory compliance, and provide excellent customer service. This role requires 5 years of experience and strong organizational skills. Responsibilities include preparing documents, reviewing shipping documentation, and...
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Senior Regulatory Specialist
hace 4 semanas
Tijuana, México Merit Medical A tiempo completo**SUMMARY OF DUTIES**Responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for Europe, the United States, and other countries. Primary responsibilities are to ensure regulatory compliance for assigned product lines Other responsibilities include coordinating recalls, identifying relevant standards and...
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hace 5 días
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