Regulatory Affairs Jobs in India

Job DescriptionIdentify and develop new business opportunities in and nbsp;international markets (Asia Africa LATAM CIS Europe etc.)Manage and grow relationships with and nbsp;existing overseas clients distributors and partnersHandle and nbsp;export documentation quotations and tender submissionsCon...

The role involves monitoring and analyzing regulatory and policy developments in the renewable energy sector preparing internal advisories and supporting the Lead in policy advocacy initiatives. This job involves certain external meetings focusing on research documentation and compliance tracking.Ke...

Job SummaryWe are seeking a dynamic and experienced Team Lead in Process Development to lead and guide the Injectable Process development team in areas of Quality by Design (QbD) Process selection Scale Up and Technology transfer to Manufacturing Science & Technologies (MSAT)/ Formulation Technology...

Job SummaryWe are seeking a dynamic and experienced Lead in Process Development provide technical leadership in ideating strategizing and developing novel formulations to build differentiated product portfolio for serving unmet needs of patients. Ensuring successful establishment of proof of concept...

Job Summary As part of the GIEEE Finance & Administration Internal Audit Department the Internal Auditors primary responsibility is the execution of an annual risk-based audit plan which will include the performance of operational financial and compliance audits of Conferences Geographic Units and o...

At Bayer were visionaries driven to solve the worlds toughest challenges and striving for a world where Health for all Hunger for none is no longer a dream but a real possibility. Were doing it with energy curiosity and sheer dedication always learning from unique perspectives of those around us exp...

Job Title: Literature Review AdvisorCareer Level - CIntroduction to role:Are you ready to make a difference in the pharmaceutical industry As a Literature Review Advisor youll be at the forefront of ensuring the quality and accuracy of comprehensive literature reviews within the pharmaceutical secto...

Job Title: Literature Review AdvisorCareer Level - CIntroduction to role:Are you ready to make a difference in the pharmaceutical industry As a Literature Review Advisor youll be at the forefront of ensuring the quality and accuracy of comprehensive literature reviews within the pharmaceutical secto...

Risk and Compliance program managementPRINCIPAL RESPONSIBILITIES:Examination Prep & Regulatory Issues: Assist with preparation coordination and execution for regulatory examinations bank audits and regulatory action items through meeting attendance information gathering and issue follow-up; manage e...

Position Summary:The Senior Clinical Data Engineer leads the strategic development and optimization of clinical data systems to support regulatory compliance advanced analytics and operational excellence across global trials. This role drives enterprise-level data standardization initiatives and arc...

Position Summary:The Senior Clinical Data Engineer leads the strategic development and optimization of clinical data systems to support regulatory compliance advanced analytics and operational excellence across global trials. This role drives enterprise-level data standardization initiatives and arc...

Position Summary:The Senior Clinical Data Engineer leads the strategic development and optimization of clinical data systems to support regulatory compliance advanced analytics and operational excellence across global trials. This role drives enterprise-level data standardization initiatives and arc...

Title - Manager - TMF Team LeadWork Location: Manyata Tech Park Bangalore IndiaWork Schedule: Three days on-site two days remote (3/2)Work Hours: 9 am to 6 pm IST or 2 pm to 11 pm IST basis business needs (Transport available as per company policy)Career Level: D - Team LeadAbout role:TheGBS TMF Man...

Title - Senior Manager - TMF Team LeadWork Location: Manyata Tech Park Bangalore IndiaWork Schedule: Three days on-site two days remote (3/2)Work Hours: 9 am to 6 pm IST or 2 pm to 11 pm IST basis business needs (Transport available as per company policy)Career Level: E - Team LeadAbout role:TheGBS...

Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to...

Role OverviewThe Liaison Executive (DTCP & CMDA) is responsible for coordinating and obtaining necessary approvals and clearances from statutory authorities such as the Directorate of Town and Country Planning (DTCP) and the Chennai Metropolitan Development Authority (CMDA) for real estate and infr...