1 Opening(s)
14.0 Year(s) To 25.0 Year(s)
30.00 LPA TO 65.00 LPA
KEY RESPONSIBILITIES
Responsible for leading the design, implementation, and maintenance of comprehensive security measures across all stages of medical device development, ensuring compliance with relevant regulations and standards while protecting patient data and device integrity
Lead the design and implementation of secure architectures for new medical devices, considering connectivity, data protection, access ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
The documents required for NABL approval for a chemist's laboratory include:
NABL 100: General information about NABL
NABL 112: Criteria for medical laboratories
NABL 126: Specific criteria for medical devices calibration
NABL 151: For testing laboratories
NABL 152: For calibration laboratories
NABL 155: Application form and checklist for NABL medical
NABL 160: Information related to the management of the quality system manual
NABL 219: Assessment forms ...
1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Job Summary:
The Testing Engineer / Senior Testing Engineer will be responsible for conducting a variety of tests to ensure the quality, functionality, and compliance of products and equipment with relevant standards and specifications. This role focuses on Vibration, IP, ATEX (Explosionproof/Flameproof), Cables and Enclosures, and Appliance Testing (including Temperature Measurement, ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
20.00 LPA TO 27.00 LPA
Job Title: Electrical Engineer - BESS (Design and Engineering)
Location: Gurugram HQ
Employment Type: Full-time
Job Summary:
We are seeking a skilled Electrical Engineer - Battery Energy Storage System (BESS) to lead the design, engineering, and implementation of Battery Energy Storage Systems. The ideal candidate will have expertise in energy storage, electrical engineering, and ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
Prepare Documents for Digital Signature regarding DGFT, ICE Gate.
Online application for Fresh, Modification & Cancellation of IEC, RCMC.
Application of Fresh, Amendment, Enhancement, Revalidation, EO Extension of Advance Authorisation.
Prepare Documents of Bond Registration and Register the Bond at Customs at port of Registration mention in Advance Authorisation.
Prepare Documents and Application of ...
1 Opening(s)
14.0 Year(s) To 19.0 Year(s)
30.00 LPA TO 45.00 LPA
Position Responsibilities:
Provide technical leadership within cross-functional project teams to lead System Integration strategic planning to achieve project and quality goals in a systematic manner
Investigate and resolve system issues, making improvements to address customer feedback and requests as well as leading verification and validation testing activities • Lead system integration on ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.20 LPA TO 4.50 LPA
Role Description:This is a full-time on-site role for a Quality Control Officer located in Vagra. The QualityControl Officer will be responsible for ensuring the consistently high quality of the company'sproducts and will be involved in the testing, analysis, and documentation of productsthroughout their development.
Must have skill:• Instrument Handling of GC, ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
0.00 LPA TO 0.00 LPA
E & I InspectorInspector shall have university degree with minimum 5 years of inspectionexperience.Inspector shall demonstrate a thorough working knowledge of the NationalElectric Code/NFPA 70, IEC or equivalent standards. He shall also haveworking knowledge of electrical installations including materials, methods,specifications, and hazardous location identification for oil and gas orpetrochemical industries.Inspector ...
1 Opening(s)
0 To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
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 ...
1 Opening(s)
2.0 Year(s) To 9.0 Year(s)
2.00 LPA TO 5.00 LPA
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 ...