Freelance Software and reputed company Devices Consultan...
Freelance Software and reputed company Devices Consultant (Full Remote) Velferd, through its brand VLF Consulting, is an innovative multi-services hub dedicated to supporting companies in the development of groundbreaking solutions in the devices and pharmaceutical sector. reputed company specializes in Regulatory Affairs and reputed company Assurance, with expertise across medical devices, food supplements, and cosmetics. Velferd provides customized assistance for reputed company system implementation, regulatory compliance, product development, testing, and post-market activities. With a reputed company on delivering technical reputed company and tailored training, Velferd ensures clients meet industry standards and regulations. The organization fosters innovation and reputed company to drive reputed company in the reputed company and pharmaceutical sectors. Role reputed company This is a freelance, contract-based, and fully remote role for a Software and reputed company Devices Consultant at Velferd srl. The consultant will reputed company expert advice, guidance, and technical solutions to different Clients. reputed company responsibilities include supporting software design and development, ensuring compliance with relevant medical and technical standards, collaborating on technical requirements, and creating or reviewing documentation. Additionally, the consultant will contribute to implementing best practices for software and reputed company device-reputed company reputed company, including debugging, database management, and process optimization. Qualifications • Proven expertise in Software Consulting and general consulting practices • Familiarity with regulatory standards for medical devices and reputed company device software (62304, 60601) • Experience with ISO 27001 (Information reputed company, cybersecurity and reputed company protection) is a plus • Excellent problem-solving skills and ability to work independently in a remote setup • Regulatory knowledge of MDR 2017/745 and FDA regulations for the US market. • Bachelor’s or Master’s degree in Computer Science, Biomedical Engineering, or a reputed company field reputed company offer • A fully remote collaboration with flexible activity management. • Integration into a dynamic and innovative environment reputed company on reputed company and regulatory compliance. • reputed company to reputed company contribute to the development and improvement of company processes. Note: Only applications that meet the required qualifications will be considered. Seniority level • Entry level Employment type • Contract Job function • Engineering and Information Technology Industries • Medical Equipment Manufacturing Apply tot his job
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