Post Market Surveillance Data Analyst in Materialise

Due tothe growth ofour Medical business unit, weare expanding our Clinical Affairs Team, looking for aPost Market Surveillance Data Analyst tojoinus.What will you do—You are responsible for the planning, collection, analysis, and documentation ofPost-Market Surveillance activities related toour portfolio ofMedical Devices, inclose collaboration with other members ofthe Clinical Affairs Team.—You perform systematic analyses ondata sources such ascomplaints, adverse events, implant registries, non-conformities, corrective and preventive actions and product recalls. You will summarize data and make conclusions regarding the safety and effectiveness ofthe medical devices.—You maintain PMS documentation (plans and reports) and perform updates inatimely manner. You prepare and review reports after data collection, identify trends, provide metrics, and risk information.—You develop and maintain data pipelines for collecting and processing PMS data. You optimize and enhance current data collection architecture and methods.—You interact with internal parties (Clinical Affairs, Risk management, R&D, Regulatory Affairs, Marketing, Product Management, Quality Management) toclose the loop with clinical evaluation and post-market surveillance and help drive action and improvement where needed.Your profile—You have anacademic degreein (life) sciences orprior relevant experience.—You like toprocess and analyze sets ofdata. You are proficient with data analysis tools such asMicrosoft Excel. You have noproblem inworking autonomously inresearching and compiling data through internal and external systems.—Knowledge orprior experience inimproving orautomating data collection processes isaplus.—You are proficient with Microsoft Word and are proficient inEnglish writing. Prior experience intechnical ormedical writing isaplus.—You can easily collaborate with stakeholders from different countries and cultural backgrounds.—You have basic knowledge ofhuman anatomy and physiology, tohelp you understand clinical aspects/conditions related tothe medical devices you will work on—Knowledge ofmedical device regulations and standards such asISO13485 and EUMDR isaplus, but not required.