Fda Regulations Jobs in Kharghar

Study Start-up and Regulatory Submission Manager Total Experience: 5 10 years in clinical research with a focus on India-specific clinical trial operations. Mandatory Expertise: Clinical Trial Applications (CTA) and Regulatory Submissions Clinical Study Start-Up Activities India More...

15 years of overall experience in the contact center domain with transformation solution and technology implementation - Working with internal and partnership ecosystem to design and build innovative contact center solutions - Support sales RM and solutions teams in building proposal More...

The senior medical writer is responsible for the content quality and timely delivery of technical documents in support of clinical study activities (Phase I to Phase IV PASS). In this role the senior medical writer will be part of a collaborative team that works with the sponsor More...

JD : - comprehensive overall understanding of government e-marketplace (gem) - deep understanding of government procurement process through government e-marketplace (gem)/e-procurement portal/cppp including addition of categories registering with the requisite portal vendor regist More...

REQUIREMENTS:Total experience 14 Years.Hands-on architecture experience using Camunda BPM. Deep expertise in BPMN DMN and CMMN standards and practical implementation.Strong programming skills in Java Spring Boot and building RESTful APIs.experience in business process automation More...

REQUIREMENTS:Total experience 14 years.Strong working experience of Pega experience with at least 3 years or 2 full implementations as a Lead System Architect (LSA).Mandatory certification: Pega Certified Lead System Architect (CLSA).Proven ability to successfully run end-to-end More...