710 Job openings found

Job Description  Senior Software Engineer - Embedded C++ , OS, I2C,SPI,UDP,DDS - (230004QX) Description   A Day in the Life  ·       Work with global R&D teams to develop software for new and existing medical device products. ·       Software design and development of embedded real-time systems, including the development of Software Unit Test & Integration plans and protocols. ·       Participates in reviews, code ...

A Day in the Life   One of the key deliverables of MIDC is an electromechanical product that will be used in a clinical setting.  We are looking for a Lead systems engineer who will work on capturing system requirements, concept design, system modelling, risk analaysis, system.  Given the entrepreneurial nature of ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results i n compliance with the Quality Management Plan & authorize their release for medical devices  Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information abou t the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

Position:          Sr. Executive/Asst. Manager -QA Location:         Vapi Experience:     4- 8 Years Industries:      Medical Device Responsibilities: Should have experience in Medical Device Coordinate with Certification body for Certification / Surveillance Audit. Conduct Internal Quality audit as per define timeline. Document and Data control by periodic review of SOPs, Formats. Develop, ...

Job Description: Knowledge of Medical device industry standard like ISO 13485: 2016, CE, CDSCO etc. would be an advantage.Responsible to prepare production planning, review as per requirements defined by Sales team Responsible to communicate with Quality, sales, purchase & marketing team as per the requirement.Shall proficient in verbal & writing communication ...

Experience to prepare and review the documentation required for the ISO 9001:2015, EN ISO 13485: 2016, Quality management System, WHO-GMP, EU MDR 2017/745, IMDR 2017. Knowledge and preparing documents such as Quality Manual, Site Master File, SOP’s, Change Control, Deviation, CAPA, Incident, and Customer complaint, Management Review Meeting, pdate Harmonized Standards, ...

Job Description Key Responsibilities • Identify and target potential customers, including hospitals, clinics, and healthcare providers. • Meet and exceed monthly, quarterly, and annual sales quotas. • Driving incremental revenue through successful sales activities • Conduct presentations and demonstrations to showcase the features and benefits of our medical devices. ...

Roles and responsibilities:1. Travel to defined geographies to sell medical equipment.2. Contact potential customers at hospitals, clinics, doctors' offices, rehabfacilities, and nursing homes to sell medical products and equipment.3. Arrange appointments with doctors, and hospital medical teams.4. Cold-call or go Customer to customer5. Deliver presentations to doctors.6. Build relationships with ...