Job Description

Job Title
Medical Device Regulatory Affairs InternRole Overview
As a Medical Device Regulatory Affairs Intern, you will support our regulatory affairs team in managing the regulatory processes for medical devices. You will assist in preparing documentation, conducting research, and ensuring compliance with regulatory requirements. This internship provides a valuable opportunity to learn about regulatory affairs in the medical device industry and gain practical experience in a supportive environment.About us
Alcotech is a company that specialises in Drug testing, Alcohol testing, Infectious Disease Kits, and Medical Device Regulatory Affairs.Interns will have the opportunity to:\xe2\x97\x8f Gain exposure to regulatory processes and requirements in a professional and dynamic setting.\xe2\x97\x8f Hands-on experience in medical device regulatory affairs and compliance.\xe2\x97\x8f Work with experienced professionals and gain insights into the medical device industry.The day-to-day activitiesAssist in preparing and reviewing regulatory submissions, including pre-market applications, technical files, and compliance reports.Conduct research on regulatory requirements and guidelines for different markets to support submission strategies and compliance.Maintain and organize regulatory documentation and track submission status and deadlines.Assist in monitoring and reporting on the performance of medical devices in the market to ensure ongoing compliance.Identify and mitigate the risks associated with the unregulated sale of medical devices on online platforms. Work closely with regulatory bodies, marketplace operators, and internal teams to ensure that all devices sold online comply with applicable laws and regulations.Work with on marketing project and conduct competitor research and identify potential market opportunities for new products.Support sales efforts by providing insights on regulatory requirements for entering new markets and advising on compliance risks.Handle diverse operational matters as needed, contributing to the overall efficiency of the regulatory affairs team.Learning Outcome1. Gain Practical Experience in Regulatory AffairsDevelop hands-on experience in preparing and reviewing regulatory submissions, maintaining documentation, and ensuring compliance with industry standards. Learn to navigate regulatory processes in the medical device sector.2. Understand Regulatory Requirements and ComplianceAcquire knowledge of regulatory guidelines and requirements for different markets. Conduct research to support compliance strategies and understand how to manage the regulatory landscape effectively.3. Enhance Professional Skills and Industry InsightsWork closely with experienced professionals to gain valuable insights into the medical device industry. Improve your organizational, research, and communication skills while contributing to the efficiency of the regulatory affairs team.RequirementsHighly organized and detail-orientedProactive team player, able to take charge and follow-throughAbility to work independently and as part of a teamAble to dedicate at least 3 months full time internshipWork EnvironmentOffice working environment
Working hours are Monday - Friday 9am - 6pmOur office address is
25 Bukit Batok crescent, #09-13 The Elitist Singapore 658066Salary: $1000 - $1,300 monthlyApplication InstructionsIf you are interested in this opportunity, please send us your resume to

InternSG