Medical Device Regulatory Operations Associate
E Merge Tech Global Services · Chennai · onsite · Posted 41d ago
Undisclosed0–4 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- Manage and coordinate medical device regulatory operations activities.
- Develop and implement effective regulatory strategies to ensure compliance with industry standards.
- Collaborate with cross-functional teams to resolve regulatory issues and improve processes.
- Conduct thorough reviews of regulatory documents and submissions.
- Provide training and guidance on regulatory requirements to internal stakeholders.
- Stay up-to-date with changing regulatory requirements and industry trends.
Disclaimer: This job posting & Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
clinical researchtechnology transferRegulatory AffairsEctdUSFDACAPAICHFormulation Developmentregulatory operationsRimProject ManagementQuality AssuranceQuality ControlResearchProduct DevelopmentResearch And Development
About E Merge Tech Global Services

E Merge Tech Global Services
Analytics & KPO
11
employees
2007
19 years old
Chennai, Tamil Nadu
India
₹3.3L PA avg
Avg at E Merge Tech Global Services
About
E Merge Tech provides knowledge-intensive solutions across scientific and legal fields, helping clients tackle complex challenges with expert services.
Industries
Analytics & KPO
Employee ratings
10 reviews
2.8/ 5
Culture
3.1
Career growth
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