Regulatory Affairs Specialist for Medical Devices

Job Description:As a Medical Device Regulatory Affairs Specialist at Dozee, you will play a pivotal role in ensuring the company's products meet regulatory requirements. Your primary responsibility will be to plan, establish, and maintain a Quality Management System (QMS) in accordance with EN ISO 13485. This involves implementing regulatory strategies for...

Job Title Principal Regulatory Affairs Specialist About the RoleWe are seeking a seasoned Regulatory Affairs professional to lead our efforts in ensuring compliance with global regulations and standards for medical devices. As a key member of our team, you will be responsible for developing and executing regulatory strategies for new product development,...

OverviewLifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. We connect professionals with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.SalaryThe estimated salary for this position is $120,000-$180,000 per annum, depending on experience and qualifications.Job DescriptionWe are seeking an...

Indegene is a technology-led healthcare solutions provider driven by a purpose to enable healthcare organizations to be future-ready. With accelerated global growth opportunities for talent that's bold, industrious, and nimble, Indegene offers a unique career experience that celebrates entrepreneurship, innovation, collaboration, and empathy.We are looking...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Dozee. As a key member of our Quality Assurance department, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.About the RoleThis is a fantastic opportunity for an experienced professional to leverage...

**Job Summary:**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Dozee. This role will be responsible for ensuring compliance with local and international regulations, including US FDA, EU MDR, and ISO 13485.The ideal candidate will have a strong understanding of medical device regulations, experience with international...

As a Regulatory Documentation Specialist at Celegence, you will play a crucial role in ensuring the timely development and delivery of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across various therapeutic areas.The ideal candidate will have a strong background in publication experience, preferably in...

Company OverviewLifelancer is a leading talent-hiring platform in the Life Sciences, Pharma, and IT sectors. Our mission is to connect top talent with opportunities in these fields. Job Title: Regulatory Affairs ManagerSalary: $120,000 - $180,000 per yearLocation: Remote or On-Site (Flexible)Job Description:We are seeking an experienced Regulatory Affairs...

Job SummaryWe are seeking a seasoned Senior Regulatory Affairs Specialist to join our dynamic team at AliveCor. As a key member of the regulatory team, you will play a crucial role in overseeing medical device development and market introduction worldwide.Your primary responsibility will be to manage product submissions, perform regulatory pre- and...

**Job Overview**">We are seeking a highly skilled Medical Device Regulatory Compliance Specialist to join our team at Dozee.As a Medical Device Regulatory Compliance Specialist, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements. You will be responsible for planning, implementing, and maintaining a...

Job Description Overview:ScaleneWorks seeks a skilled Regulatory Affairs Specialist to lead our regulatory efforts. As a key member of the team, you will be responsible for ensuring the compliance of our products with relevant regulations.About the Role:This is an exciting opportunity to join ScaleneWorks as a Regulatory Affairs Specialist. You will be...

**About Lifelancer**Lifelancer is a global talent-hiring platform that connects professionals with opportunities in the life sciences, pharma, and IT industries. Our goal is to help individuals advance their careers while promoting equal opportunities for people with disabilities. **Company Overview**Lilly is a global healthcare leader headquartered in...

**Job Overview:**We are Dozee, a leading company in the medical device industry, and we are looking for an experienced Medical Device Compliance Manager to join our team.The ideal candidate will have a strong background in medical device regulations, experience with international submissions, and excellent analytical skills.About the Role:This is a full-time...

Job Title: Regulatory Affairs SpecialistLocation: Bengaluru, Karnataka, IndiaContract Type: Full-timeSeniority Level: Mid-Senior levelAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Lifelancer. In this role, you will be responsible for ensuring compliance with various food regulations and laws in...

Pramana's Vision :Pramana aims to bring fully autonomous systems to pathology labs, enabling AI-enabled workflows for serving patients. As a key player in this ecosystem, we require a highly skilled Cybersecurity Professional to ensure our digital solutions meet regulatory requirements.Job Description :Work closely with cross-functional teams to ensure...

About the RoleWe are seeking a highly skilled Regulatory Affairs Strategist to join our team at ResMed. As a key member of our regulatory function, you will play a vital role in ensuring compliance with multiple regulatory frameworks and supporting the design, development, and manufacture of products that meet our customers' quality requirements.Key...

About the Role:Dozee is seeking a highly skilled Regulatory Compliance Expert - Medical Devices to join our team. As a Regulatory Compliance Expert, you will be responsible for ensuring that our medical devices meet regulatory requirements. This includes planning, establishing, and maintaining a Quality Management System (QMS) in accordance with EN ISO...

Baxter is a leading global innovator of medical products, with a legacy spanning nearly 70 years. Our journey towards separating the $5B Kidney Care segment into a standalone company has brought about an exciting opportunity to revolutionize kidney care and other vital organ support.As a Regulatory Affairs Specialist for Kidney Care Product Development, you...

Vantive: Revolutionizing Kidney CareBaxter is transforming its Kidney Care segment into a standalone company, Vantive. This new entity will leverage Baxter's legacy in acute therapies and home and in-center dialysis to deliver best-in-class care to patients worldwide.As a Regulatory Affairs Specialist at Vantive, you will be part of a community driven to...

About the OpportunityGainwell Technologies is a leading technology company that values innovation and excellence. We are seeking a Regulatory Affairs Specialist to join our team and play a critical role in ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and update compliance policies and procedures.Disseminate regulations to...