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.
Job description
As a global mdr submission analyst ii osta team member, you will be responsible for timely regulatory reporting assessments and reassessments of global complaints, preparation and submission of initial /supplemental/ importer mdr reports for post market activities per 21cfr803Perform follow-up to obtain additional information for adverse events by collaborating with field specialists, sales representatives, engineers, technicians, clinicians, and customers directlyPerforms routine assignments with minimal direction from manager; requires general instruction for new or special assignments from managerThis position will be able to speak and read japaneseThe analyst ii will maintain quality documents to ensure compliance with global medical device guidance documentsThe analyst ii requires working knowledge of medical device quality systems regulations including iso 13485, 21cfr820, and 21cfr803This is a field/remote position and there are multiple openings available.
Job duties
Review incoming complaints to determine the facts of the case.
Verify information including information available in ancillary systems data sources(for example: datasweep, sap)
Performs follow-up to obtain additional information for adverse events by collaborating with field specialists, sales representatives, engineers, technicians, clinicians, and customers directly.
Conducts timely initial mdr reportable assessment/ submission per 21cfr803.
Conducts timely re-assessments when new information has been received to determine if an initial or supplemental mdr is required per 21cfr803.
Assist with preparation and submission of fda additional information responses, and associated documentation to the fda and manufacturing business centers (mbcs).
Assist global mdr submission management in the successful identification and resolution of quality issues associated with complaints.
Key team player working closely with other global mdr submission associates.
Perform other duties as assigned
Job requirements
Required qualifications:
Bachelor of science degree with a minimum of 1-3 years medical device experience or an associate`s degree with scientific discipline with a minimum of 3-5 years medical device experience (i.eAssociate rn, x-ray technician, biomedical technician)
Complaint handling/ customer service experience in the medical device/ pharmaceutical required.
Effective communication skills - both written and verbal english language.
Ability to effectively prioritize and manage workload.
Knowledge/ ability to utilize various software/ database sources.
Must be able to maintain good attendance regular scheduled hours.
Must be able to follow standard practices and procedures.
Attention to detail and accuracy required.
Strong analytical and organizational skills required.
Must be able to prioritize workload in order to meet regulatory/ procedural deadlines.
Preferred qualifications:
Basic knowledge of medical terminology and human anatomy.
Demonstrated working knowledge of medical device quality systems regulations including iso 13485, 21cfr820, and 21cfr803.
Applies professional concepts and company policies and procedures, analyzes data or situations, and exercises judgment to recommend solutions to solve problems.
Follows standard practices and procedures in analyzing situations or data from which answers can be obtained.
We realize work isn’t just a job to you.
It’s a big part of your life, but not the only partThat’s why we offer competitive salaries, a robust 401(k) program, 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 passionate about the solutions it creates for the medical, life sciences, and industrial equipment industries, as well as cameras and audio productsFor more than 100 years, olympus has focused on making people’s lives healthier, safer and more fulfilling by helping detect, prevent, and treat disease, furthering scientific research, ensuring public safety, and capturing images of the world.
Olympus’ medical business uses innovative capabilities in medical technology, therapeutic intervention, and precision manufacturing to help healthcare professionals deliver diagnostic, therapeutic, and minimally invasive procedures to improve clinical outcomes, reduce overall costs, and enhance the quality of life for patientsOlympus’ medical portfolio includes endoscopes, laparoscopes, and video imaging systems, as well as surgical energy devices, system integration solutions, medical services, and a wide range of endotherapy instruments for endoscopic and therapeutic applicationsFor more information, visit www.olympus-global.com.
Olympus…true to youTrue to societyTrue to life.
It is the policy of olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.
Posting notes: || united states (us) || tennessee (us-tn) || bartlett ||
