Empleos actuales relacionados con Medical Device Surveillance Specialist Role - San José, San José - Microport Orthopedics S.A.
-
Medical Device Surveillance Specialist
hace 2 semanas
San José, San José, Costa Rica Microport Orthopedics S.A. A tiempo completoAbout the RoleAt MicroPort Orthopedics S.A., we are driven by a passion for innovation and a commitment to excellence. As a Medical Device Surveillance Specialist, you will play a critical role in ensuring the safety and effectiveness of our medical devices.
-
Medical Surveillance Specialist
hace 1 semana
San José, San José, Costa Rica Pfizer A tiempo completoJob SummaryWe are seeking a skilled Medical Surveillance Specialist to join our team. The successful candidate will be responsible for monitoring drug, biologics and medical devices surveillance programs.The ideal candidate will have a strong background in pharmacovigilance and safety data analysis. They will also possess excellent organizational skills,...
-
Medical Device Specialist
hace 1 semana
San José, San José, Costa Rica Boston Scientific A tiempo completoCompany OverviewBoston Scientific is a leading medical device company with over 40 years of experience in solving complex health challenges. Our mission is to advance science for life, transforming lives through innovative medical solutions that improve patient outcomes and create value for our customers.
-
Medical Device Support Expert
hace 2 semanas
San José, San José, Costa Rica Boston Scientific Corporation A tiempo completoJob DescriptionThe Field Clinical Specialist I position at Boston Scientific Corporation requires a highly skilled professional who can provide clinical support and assistance to our customers in Costa Rica. As a key member of our team, you'll be responsible for:Maintaining consumption records and creating value through in-service presentations and product...
-
Emergency Medical Specialist
hace 2 días
San José, San José, Costa Rica Aspen Medical A tiempo completo**Emergency Medical Specialist Job Summary**We are seeking an experienced Emergency Medical Specialist to join our team. As a key member of our healthcare team, you will provide advanced medical care to patients in emergency situations and collaborate with other healthcare professionals to ensure seamless patient care.**Responsibilities**The responsibilities...
-
Medical Device Validation Specialist
hace 1 semana
San José, San José, Costa Rica Gsb A tiempo completoAbout UsGsb is a leading company in the medical device industry, committed to delivering high-quality products and services. Job DescriptionThis role involves providing technical support and guidance to ensure that all processes and equipment meet regulatory requirements. Key ResponsibilitiesDevelop and implement technical proceduresConduct training sessions...
-
Medical Device Regulatory Expert
hace 6 días
San José, San José, Costa Rica Smith+Nephew A tiempo completoEmpowering Patients through Innovative SolutionsAt Smith+Nephew, we strive to create meaningful connections between patients and our life-changing technologies. As a key member of our team, the Regulatory Affairs Specialist II will play a vital role in shaping our regulatory approach, ensuring seamless product introductions, and maintaining market presence...
-
Medical Device Sales Representative
hace 2 semanas
San José, San José, Costa Rica Medtronic A tiempo completoAbout the RoleWe are seeking a highly motivated Medical Device Sales Representative to join our team. As a key member of our sales team, you will be responsible for promoting and selling Medtronic's products and services within an assigned geographic area and/or specific customer accounts.ResponsibilitiesPromote and sell Medtronic's products and services to...
-
Product Surveillance Specialist
hace 2 semanas
San José, San José, Costa Rica Zimvie A tiempo completoWelcome to ZimVie, a new, publicly traded global company focused on improving quality of life for our patients.Our company is founded on a legacy of established brands, medical experts and over $1B in annual revenue.We design, manufacture, and distribute a comprehensive portfolio of innovative solutions for implant dentistry, spinal surgery and bone growth...
-
Campaigner - Surveillance
hace 5 días
San José, San José, Costa Rica Access Now A tiempo completo**The Organization and Role***About Access Now*Access Now is a growing international human rights organization dedicated to defending and extending the digital rights of users at risk around the world, including issues of privacy, security, freedom of expression, and transparency.Our policy, advocacy, technology, and operations teams have staff presences in...
-
Clinical Research Analyst
hace 2 semanas
San José, San José, Costa Rica Microport Orthopedics S.A. A tiempo completoResponsibilities and ExpectationsThe ideal candidate will have:A strong understanding of medical device regulations and guidelines.Excellent analytical and problem-solving skills, with the ability to interpret complex data and draw meaningful conclusions.Strong communication and interpersonal skills, with the ability to work effectively with cross-functional...
-
Medical Device Post Market Surveillance Specialist
hace 20 horas
San José, San José, Costa Rica Microport Orthopedics S.A. A tiempo completoCompany Overview: At MicroPort Orthopedics, we are dedicated to advancing the field of orthopedics through innovation and collaboration. Our mission is to help patients achieve full function and mobility through cutting-edge medical devices.
-
Medical Device Program Manager
hace 4 días
San José, San José, Costa Rica Johnson & Johnson A tiempo completoCompany Overview">Johnson & Johnson MedTech is a global leader in the medical device industry, dedicated to transforming healthcare through innovative solutions. With a rich history of pioneering and innovation, we have been impacting the health of over 1 billion patients and consumers every day for more than 130 years.">Salary and Job Description">We are...
-
Medical Device Regulatory Associate
hace 7 días
San José, San José, Costa Rica Zimvie A tiempo completoJob SummaryWe are seeking a highly motivated Medical Device Regulatory Associate to join our team. As a key member of our regulatory department, you will be responsible for assisting in the preparation of technical documentation for regulatory submissions worldwide. Your role will also involve researching and analyzing information related to regulatory...
-
Medical Device Validation Manager
hace 1 semana
San José, San José, Costa Rica Gsb A tiempo completoJob SummaryGsb is seeking an experienced Life Cycle Management Engineer to join our team. In this role, you will be responsible for managing the entire product lifecycle, from development to launch and beyond. The successful candidate will have a strong background in engineering, project management, and quality assurance.The ideal candidate will have a...
-
Medical Professional
hace 1 semana
San José, San José, Costa Rica Aspen Medical A tiempo completo**About Aspen Medical**: We are a market leader in providing medical support to cruise lines. Our team of experienced physicians provides high-quality care to guests and crew onboard our ships.Job DescriptionWe are seeking a highly skilled Emergency Care Specialist to join our team. As a physician on one of our cruise ships, you will be responsible for...
-
Maritime Medical Specialist
hace 2 semanas
San José, San José, Costa Rica Aspen Medical A tiempo completoAspen Medical is seeking qualified Nurses to fill key positions onboard cruise ships.In this role, you will be responsible for delivering exceptional patient care, working closely with colleagues to ensure seamless service delivery.Essential Qualifications:Nursing Degree and relevant experienceALS certification and 3 years of post-qualification...
-
Medical Device Regulatory Specialist
hace 2 semanas
San José, San José, Costa Rica Zimmer Biomet A tiempo completoOur company overview highlights our commitment to innovation and customer satisfaction. We strive to provide mobility and renewed life to people around the world through our products and services.The Regulatory Affairs Specialist is responsible for obtaining sanitary registration for the product portfolio by assembling, distributing, storing, and tracking...
-
Technical Support and Surveillance Expert
hace 2 semanas
San José, San José, Costa Rica Grupo Stt A tiempo completoAbout UsGrupo Stt is a leading provider of GPS tracking systems, MDVR video surveillance solutions, and CCTV installation services. Our mission is to deliver exceptional customer experiences through our expertise and dedication.Job SummaryWe are looking for a skilled Technical Support Engineer to provide top-notch support to our clients. The successful...
-
Pm Surveillance Engineer I
hace 3 semanas
San José, San José, Costa Rica Microport Orthopedics S.A. A tiempo completoAt MicroPort Orthopedics, we are never standing still.We know that knee and hip implants are constantly being improved just as medical procedures themselves evolve with each passing day.We not only embrace this constant advance in medicine.We celebrate it in our work.We operate with the heart of a start-up but the soul of an industry powerhouse.This is...
Medical Device Surveillance Specialist Role
hace 2 semanas
Job Overview:
MicroPort Orthopedics S.A. is seeking a highly skilled Post-Market Surveillance Engineer to join our team. As a PMS Engineer, you will play a critical role in ensuring the safety and effectiveness of our orthopedic products.
Main Responsibilities:
- Conduct thorough analyses of product complaints, determine trends, and summarize the findings in accordance with established procedures and regulatory requirements.
- Schedule and facilitate PMS review team meetings, prepare meeting minutes, and ensure timely completion of action assignments.
- Assist the Regulatory Affairs group with new product submissions and license renewals by providing results from PMS review findings and answering questions from government agencies.
- Support Product Development Engineers in developing Design FMEA and Risk Analysis plans for new products under development and review their work.
Key Activities:
- Organize and conduct PMS meetings according to the established meeting schedule.
- Prepare complaint rates and complaint trends reports to provide key analysis of product safety.
- Conduct searches and reviews of published information, providing summary reports on clinical data for MPO and competitive products.
- Assist in writing initial Clinical Evaluation Reports.
- Review Device Registries and government databases for MPO and competitive products.
- Write and distribute summary PMS reports and update the electronic database.
- Routinely update CERs with new PMS data after each PMS review.
- Provide training on the Post Market Review procedure and database keeping to new employees.
Skills and Qualifications:
- Familiarity with basic orthopedic knowledge to read and comprehend published scientific literature.
- Strong leadership skills, excellent analytical and problem-solving abilities, good communication skills, and technical writing skills.
- Entry-level with a strong engineering background and independent research skills.
- Ability to work well within a team environment and balance multiple ongoing projects, timelines, and outputs.
Requirements:
- Minimum 1 year of related experience, including a combination of internship and/or research experience.
- Some experience in the medical device industry with a focus on clinical research, quality, reliability, or development engineering is preferred.
- Bachelor's Degree in a Science/Engineering/Technical or related degree required; Master's Degree preferred.
