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4.0 - 8.0 years
0 Lacs
pune, all india
On-site
As a candidate for the position, you will be responsible for the following: Role Overview: You will be involved in design, configurations, and development using Opcenter EX Core, MDD, Semi, and Electronics. Additionally, you must have hands-on experience with Designer, Portal Studio, and Connect MOM. Your knowledge should cover both front-end and back-end development, with solid skills in Visual Studio, Rest API, and OData protocols. Experience using Mendix for UI is essential, and having the Mendix advanced certification would be beneficial. You will also need expertise in enterprise application integration, particularly with SAP/PLM, and machine integration. Proficiency in writing SQL stor...
Posted 5 days ago
10.0 - 12.0 years
0 Lacs
pune, maharashtra, india
On-site
Job Description Job title: You are a part ofu00A0the Ultrasound R&D team - Pune. Philips HIC, Pune, is playing a key role in Philips global strategy for Ultrasound. With Philips HIC, the foundation was laid to touch billions of lives and reiterate Philips commitment towards Indian and growth healthcare markets. Your role: Defining, for products to be developed, the applicable safety standards and regulations such as IEC 60601 series and/or IEC 62304, IEC 62366, the new EU MDR, and Particular Standards IEC60601-2-37, and in particular EMI/EMC IEC 60601-1-2 standards and testing Defining within the Standards and Compliance plan how the required standards and regulations will be covered in evid...
Posted 4 months ago
8.0 - 13.0 years
15 - 27 Lacs
Ahmedabad
Work from Office
Role & responsibilities Degree in Marketing, Sciences, Biomedical Engineering, or related discipline. Medical Device Certification Business experience preferred. About 8 years of experience with a Medical Devices manufacturer and / or Notified Body including about 2 years in Sales desirable. Good Communicator & writing skills. Social Media selling exposure. Well-read and updated on the Medical Device Sector happenings. Experience with ISO 13485, MDSAP, MDD, MDR, IVDR certifications. Establish rapport and liaison with Regulatory bodies and seek advance information on legal/regulatory introduction/amendments. Connects and actively interacts with Medical Device Industry forums. Generates propos...
Posted 6 months ago
8 - 13 years
12 - 18 Lacs
Hyderabad
Work from Office
Bachelors degree in Engineering 8+ years of quality systems experience Experience in Process Development, Validation& MSA, is Mandatory Working knowledge of auditing experience to the FDA Quality System Regulation, ISO 13485, and the MDD
Posted 7 months ago
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