Regulatory Affairs Associate- Medical Devices - Chennai

We are seeking a Hardware Engineer with experience in testing medical devices to join our team at Quest Global.We believe that our company culture is the key to making a true difference in every industry we reach. · ...

Quest Global is seeking a Hardware Reliability Test Engineer for medical devices with critical life-saving clinical applications. · ...

We are Hiring · Medical Equipment & Devices Sales Representative · Contact : Nithish (HR) – · Greetings from Ababil Healthcare Pvt Ltd · We are currently hiring Sales Engineers for our Medical Equipment & Devices division. If you have a background in medical device sales or are ...

We are Hiring · Medical Equipment & Devices Sales Representative · Contact : Nithish (HR · Greetings from Ababil Healthcare Pvt Ltd · We are currently hiring Sales Engineers for our Medical Equipment & Devices division. If you have a background in medical device sales or are a r ...

This is a full-time remote role for a Medical Device Regulatory Intern at PregEase. · Experience in regulatory compliance and quality assurance in the medical device industry (students are welcome) · Strong attention to detail and organizational skills · ...

Professional Summary: · Position: Medical Device Cybersecurity Expert | Embedded Systems (Linux/C/C++) | Secure Development, Risk Management | FDA, EU MDR, IMDRF Compliance · Location: Chennai · Exp.:11+ years · Industry Experience: 12+ years of professional experience, with ove ...

Install and maintain medical equipment. Perform preventive maintenance checks and provide technical support to healthcare professionals. · Maintain accurate service records. · Ensure compliance with regulatory requirements. · ...

We are currently hiring Sales Engineers for our Medical Equipment & Devices division. If you have a background in medical device sales or are a recent Biomedical graduate eager to begin a career in this exciting field, we encourage you to apply. · ...

+ Medical device cybersecurity expert with 12+ years of experience in medical device cybersecurity and regulatory compliance. · + · ...

We are looking for a motivated Field Sales Associate to grow our presence across hospitals and clinics in Chennai. · Drive on-ground sales through clinic and hospital visits · Conduct product demos and support patient fittings · ...

Design new medical devices or improve existing ones from initial ideas to functional prototypes. · ...

Minimum 9+ years of experience in Medical Device Testing/other electronic devices testing with embedded testing knowledge. · • Should be ready to work from Chennai office all 5 days of the week. · • Lead and Mentor: Guide, coach, and provide technical direction to a team of Manua ...

Senior Technical Architect with experience in medical devices and renal dialysis machines required. Must have hands-on experience in all phases of the medical device life cycle and proficiency in plastic, sheetmetal, and machined part design. · ...

This is a full-time hybrid role for a Regulatory Affairs Associate focusing on medical devices- QMS & EU MDR compliance. · Experience with Quality & Regulatory Documentation in compliance with ISO 13485 & EU MDR/ IVDR and expertise in preparing accurate regulatory records · Profi ...

Design and develop medical devices using CAD and prototyping. · ...

➔ Job Description: Sales Representative for an Imported Medical Device · ➔ Location: Chennai · ➔ Experience: 6+ Years in Medical Device Sales · ➔ Work Hours: 9:00 AM - 5:30 PM (Includes frequent field travel) · Role Overview · We are seeking to hire a Sales Representative to spea ...

We are looking for sales engineer in our Chennai region. · Look after the alloted region sales . · prepare reports based on sales performed · AMC and CMC contractsMeet up with customers daily in order to penetratePASSION TO WORK LONG TERM AND TRAVEL WILLINGNESS. ...

The QA Associate will support the maintenance and continuous improvement of the ISO 13485 Quality Management System (QMS) for EU MDR–compliant medical devices. · Support the maintenance of the QMS in compliance with · EU MDR and ISO 13485 · ...

The QA Associate will support the maintenance and continuous improvement of the ISO 13485 Quality Management System (QMS) for EU MDR–compliant medical devices. · ...

We are looking for an experienced Regulatory Affairs Specialist with strong exposure to medical device or IVD manufacturers in India who export their products to advanced regulated markets such as USA (FDA), Europe (EU MDR/IVDR), Japan (PMDA), Australia (TGA), India Regulatory an ...