1,532 regulatory affairs intern jobs in India.

... requirements. Collaborate with international Regulatory Affairs teams and business partners to address medical and clinical regulatory queries. Represent medical affairs in regulatory meetings across regulated and emerging markets. C. International Medical Affairs & Medico-Marketing Develop and implement medical affairs strategies ...

Manager Regulatory Affairs | Mumbai/Vadodara| Hybrid (Global Regulatory Affairs / EU / RoW Regulatory Framework/Regulatory Dossier & Submission Expertise – MAA, NDA, ACTD, CTD (M1–M3) Lead regulatory activities to support the development, registration and ongoing maintenance of pharmaceutical products across relevant markets. ...

... System Requirement Job Description - Policy Advocacy & Regulatory Intelligence : Monitor, interpret, and analyze central and state policies, tariff orders, regulatory developments, and case laws impacting renewable energy assets (solar, wind, hybrids, BESS). - Strategic Development Support: Provide regulatory due diligence, ...

... Ensure compliance with IDMP (Identification of Medicinal Products) standards and evolving regulatory requirements. • Support the electronic submission of regulatory data to EMA (European Medicines Agency). • Collaborate with cross-functional teams, including Regulatory Affairs, IT, and Compliance, to ensure data consistency ...

... high-quality regulatory suitability and compliance evaluations of Döhler articles in certain countries and regions (global scope), triggered either by customer or internal stakeholder requests Maintain results of regulatory checks in the substance database Develop expertise in existing IT regulatory compliance tools and collaborate ...

... high-quality regulatory suitability and compliance evaluations of Döhler articles in certain countries and regions (global scope), triggered either by customer or internal stakeholder requests Maintain results of regulatory checks in the substance database Develop expertise in existing IT regulatory compliance tools and collaborate ...

Regulatory Affairs Specialist at Thermo Fisher Scientific supporting preparation of regulatory documentation and submissions under EUCTR guidance. The role involves coordinating client deliverables, managing project communications, and ensuring compliance with regulatory standards and internal procedures. Responsibilities ...

... in Delhi, 2022. What we want you to do : - Assist in preparing documents relating to quality management systems and regulatory submissions - Collaborate with internal departments to gather necessary information for regulatory submissions. - Provide administrative support to the regulatory affairs team as needed. What are ...

... largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, ...

... global regulatory plans and sustaining variation deliverables Requirements - Master's degree in related scientific discipline (PhD advantageous) - 7+ years regulatory affairs or healthcare experience - Regulatory Information Management systems expertise and data compliance knowledge - CMC regulatory authoring experience ...

Abbott seeks an Assistant Manager in Regulatory Affairs to develop and maintain global labeling documents, support product compliance across markets, and coordinate regulatory submissions. The role involves managing labeling portfolios, supporting affiliate regulatory activities, and ensuring adherence to international ...

... coordinating responses to regulatory authority queries. - Engage with Global Business Unit Regulatory teams and Regional Regulatory Affairs teams to ensure regulatory activities are aligned with business objectives and requirements. - Partner with regulatory affairs sub-functions to provide seamless regulatory support to ...

... global regulatory plans and sustaining variation deliverables Requirements - Master's degree in related scientific discipline (PhD advantageous) - 7+ years regulatory affairs or healthcare experience - Regulatory Information Management systems expertise and data compliance knowledge - CMC regulatory authoring experience ...

... Timely, effective and transparent communication with global stakeholders for all requests Technical expertise - - High standard of technical understanding of regulatory requirements for raw materials within all categories of use (Cosmetics, OTC, Drugs, Food/Nutritional’s etc.) - Knowledge of toxicology & safety assessment ...

... requirements are met for regulatory submissions - Timely, actively support query responses - Engage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements - Interface and align with other regulatory affairs sub-functions to provide ...

... International Regulatory Compliance, s, Medical Device Regulations, New Product Development, New Product Qualification, People Leadership, Pharmaceutical Regulatory Affairs, Product Registrations, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory CMC, Regulatory Compliance, Regulatory Experience, ...

... compliance priorities. - Develop effective stakeholder engagement strategies to resolve regulatory issues and facilitate project execution. Must-Have Skills - Regulatory Affairs: Extensive experience in regulatory strategy, policy interpretation, statutory approvals, and regulatory engagement within the power or renewable energy ...

... post-market regulatory activities, including field actions, vigilance-related submissions, product updates, and compliance requests as required. · Maintain regulatory records, databases, and document repositories in accordance with internal procedures and document control requirements. · Track changing regulatory requirements ...

Beckman Coulter Life Sciences seeks a Commercial Regulatory Affairs Specialist to manage import licenses, renewals, and post-approval applications for medical devices and IVDs across India, Sri Lanka, and South Asia. The role involves regulatory submissions, authority correspondence, cross-functional collaboration, and ...

... least 6 years of experience in regulatory affairs or regulatory labeling, preferably within the pharmaceutical, clinical research, or healthcare industries. - Regulatory Knowledge: Strong understanding of medicinal product labeling requirements, Health Authority submission processes, and regulatory procedures, including Centralized, ...