Jobs: regulatory affairs in medical device

**Company Overview**: **Sunfox Technologies** is a forward-thinking and innovative medical device company committed to revolutionizing healthcare through advanced technologies. We are seeking a talented and motivated Medical Device Regulatory Affairs Executive to play a vital role in ensuring regulatory compliance for our cutting-edge medical devices. If you...

We are Hiring Regulatory Affairs Specialist for Medical Devices (Orthopedic Implants and Instruments) Role & Responsibilities: 1. Documents preparation for ISO13485, CE Certificate (EU MDR), USFDA. 2. Work on technical master file. 3. Work on CERs (clinical evaluation report) as per MDR. 4. Have knowledge about QMS (quality management systems). 5....

We are Hiring Regulatory Affairs Specialist for Medical Devices (Orthopedic Implants and Instruments) Role & Responsibilities: 1. Documents preparation for ISO13485, CE Certificate (EU MDR), USFDA. 2. Work on technical master file. 3. Work on CERs (clinical evaluation report) 4. Have knowledge about QMS (quality management systems). 5. Reporting to...

Reporting to: Assistant Manager – Regulatory Affairs Division: Ortho Implants Location: Chennai No. of Positions: 1 Education: B.E/ B. Tech in Biomedical Engineering / M. Pharm Regulatory Affairs Experience: 2 - 4 years Exp. in ‘scientific writing / clinical documentation’ role preferred KEY RESPONSIBILITIES: Technical writing, literature search,...

Reporting to: Assistant Manager – Regulatory Affairs Division: Ortho Implants Location: Chennai No. of Positions: 1 Education: B.E/ B. Tech in Biomedical Engineering / M. Pharm Regulatory Affairs Experience: 2 - 4 years Exp. in ‘scientific writing / clinical documentation’ role preferred KEY RESPONSIBILITIES: Technical writing, literature...

Job Description:It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions.We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and...

Job Description: It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and...

Job Description:It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions.We are looking for aSr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and Medical...

Job Description: It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and...

Job Description:It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions.We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and Medical...

Job Description:It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions.We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and Medical...

Job Description: - Responsible for writing clinical evaluation reports. - Able to interpret, analyse and draw conclusions from the clinical data obtained from clinical trials, literature, etc. - Responsible for preparing software documentation - Responsible for preparing technical documentation for regulatory compliance (EU MDR, CDSCO) - Responsible for...

Responsible for writing clinical evaluation reports. - Able to interpret, analyse and draw conclusions from the clinical data obtained from clinical trials, literature, etc. - Responsible for preparing software documentation - Responsible for preparing technical documentation for regulatory compliance (EU MDR, CDSCO) - Responsible for preparing usability...

Regulatory Affairs (Medical Device) Technical/Functional Skills: The Regulatory Affairs Specialist should provide direct Worldwide Regulatory support to various projects and products. Candidate should support strategic planning and product development efforts, and provide Regulatory support for existing products with respect to product changes/modifications,...

Regulatory Affairs (Medical Device) Technical/Functional Skills: The Regulatory Affairs Specialist should provide direct Worldwide Regulatory support to various projects and products. Candidate should support strategic planning and product development efforts, and provide Regulatory support for existing products with respect to product...

The **Regulatory Affairs Specialist** stays with the same company for an average of 10 to 15 years; the rate of turnaround is therefore low. Networking is very much encouraged, through joining various associations to participate in conferences and exhibitions, and also to access current literature. Presently, there is a strong demand for Regulatory Affairs...

Job Description We are seeking a Regulatory Affairs Specialist to support a leading medical device company in Ithaca, NY. This is an onsite role open to local candidates.  Job Summary: This position will support worldwide regulatory registrations for our current and future medical devices as well as support process compliance in conjunction with our...

We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collation and...

Sunrise Remedies Job Opening for Regulatory Affairs (RA). **Experience**: Minimum 2 Years **Industries**: Pharmaceutical Company **Education**: B.Sc. / M.Sc / B.Pharm / M.Pharm **Job Location**: Santej Ahmedabad. **Key Responsibilities**: - Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices,...

We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collation and...