Associate MDR/Vigilance Specialist

About Your New Employer:

• Join a company renowned for its innovation and commitment to improving patient outcomes.
• Work with the latest advancements in medical devices and drug surveillance.
• Be part of a team that values collaboration and professional growth.

About Your New Job as MDR Specialist:

• Oversee the company's drug or medical devices surveillance program, including intake, protocol development, evaluation, processing, and follow-up on adverse reports.
• Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data, or adverse reaction data as required by regulatory agencies.
• Review and analyze clinical databases for the extraction of ADE data, ensuring the creation of a unified database consistent with ADE standardization and internalization.
• Act as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.
• Identify and address problems that are not immediately evident but typically not difficult or complex.

What Skills You Need for MDR Specialist:

• Requires broad theoretical job knowledge typically obtained through advanced education.
• Requires a Bachelor degree.

What's on Offer for MDR Specialist:

• Attractive compensation package.
• Opportunities for growth and advancement within the company.
• Work with cutting-edge technology and a team of dedicated professionals.

What's Next

Apply now by clicking the "Apply Now" button or contact Karolina at

If the job isn't quite right but you are looking for something similar, please get in touch. We also have multiple Temp, FTC, and Contract jobs available.