Medical Devices Regulatory Jobs in Pune
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Tata Elxsi - Pune, Maharashtra, India
Tata Elxsi works with leading medical device OEMs and technology companies for market research and human factor engineering, hardware and software engineering, verification & validation, regulatory
from: linkedin.com (+1 source) - 23 days ago
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Birlasoft - Pune, Maharashtra, India
all aspects of process development and execution. Exposure to Medical Devices Industry and delivered projects in that space with knowledge around UDI and Regulatory Hub. Competent and proficient understanding
from: linkedin.com (+1 source) - 25 days ago
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Pune, Maharashtra, India
’ experience working in Regulatory Affairs within medical device/technology environments, with 8+ years’ as a functional leader and strong track-record successfully leading a Regulatory Affairs teams bringing
from: jobleads.co.in (+1 source) - 5 days ago
Operon Strategist - Pune
connections with important players in the target markets, such as distributors, regulatory organizations, producers of medical devices, and healthcare providers.3. Develop and execute plans to enter new markets
from: updazz.com - 19 days ago
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Pune, Maharashtra, India
and Validation) activities, generating, and analyzing test reports Understanding of global medical device regulatory environments and clearance processes. Effective communication, computer, documentation
from: jobleads.co.in (+1 source) - 28 days ago
Philips - Pune, IN
in Mechanical, Electrical, Electronics or Mechatronics Engineering 8+ years in engineering, initially as engineer and later as technical project leader Experience in Medical Device development and knowledge
from: jobvertise.com - More than 30 days ago
Philips - Pune, IN
in Quality Assurance / Quality Control Activities in Medical devices industry preferred Technical/Functional Competencies: Working knowledge in the following quality areas: inspection, product disposition
from: jobvertise.com - More than 30 days ago
Overseas Information - Hybrid - Pune
Immediate- 30 Days. (Don't apply if you have 60/90 days NP) Key Responsibilities: Experience of 5-8 years in the Medical device industry. Exposure to good Documentation Practices and understanding of Design 5-11 Lacs PA INR
from: naukri.com - 18 days ago
Philips - Pune
. Create functional requirement documentation. Experience in Medical Device development and knowledge of IEC 60601 standards will be an added advantage. Knowledge of Global Medical Quality and Regulatory Not disclosed INR
from: naukri.com - 26 days ago
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