Regulatory Submission Manager - Bengaluru

The Senior Regulatory Submission Manager is responsible for overseeing the planning compilation publishing and dispatch of regulatory submissions to Health Authorities throughout the product lifecycle This role ensures compliance with regulatory standards and optimizes submission ...

The job holder is responsible for managing end-to-end regulatory lifecycle submissions across multiple markets, ensuring timely delivery and compliance with regulatory authority requirements, guidance and GSK processes. · ...

The job holder is responsible for managing end-to-end regulatory lifecycle submissions across multiple markets. · Own end‑to‑end delivery of assigned complex lifecycle regulatory submissions. · Provide peer review and quality assurance of deliverables. · Lead drafting and technic ...

You will be responsible for managing and overseeing end-to-end content submission processes while ensuring submissions are timely, accurate, and compliant with given Brand/AMA guidelines. · ...

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. · We celebrate all dimensions of diversity and believe that it drives excellence and innovation, · strengthening our ability to lead in science and technology.Covers regulatory p ...

We are looking for a detail-oriented and proactive Inside Sales Executive – Tendering to manage end-to-end tendering activities. The ideal candidate will coordinate across departments, ensure timely and compliant submissions, and support the business in securing new opportunities ...

The Regulatory Project Manager is responsible for global regulatory planning and tracking of regulatory deliverables for moderate-to-highly complex submissions to health authorities worldwide (including submission planning).Creates project plan for initial CTA/IND, MAA/NDA/BLA an ...

Deliver end-to-end submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines. · ...

Job Title: · Regulatory Affairs Executive – ICSR & Aggregate Reporting · Experience: · 3–5 Years · Employment Type: · Full-time · Location: · Bangalore · Role: · We are seeking a detail-oriented Regulatory Affairs professional with 3–5 years of experience in regulatory submission ...

We are seeking a highly experienced and meticulous Manager - Regulatory Affairs to oversee and execute all regulatory activities for drug substances and products. The ideal candidate will be responsible for the preparation, submission, and management of various regulatory documen ...

Job Title: Regulatory Affairs Associate – ICSR & Aggregate Reporting · Location: Remote / Bangalore · Experience: 3–5 years · Employment Type: Full-time · About the Role · We are seeking a detail-oriented and experienced · Regulatory Affairs Associate · with hands-on expertise in ...

We are looking for an experienced Technical Support Specialist with strong expertise in pharmacovigilance (PV) systems. · Experience: 4-8 years in PV systems technical support and configuration. · Technical Expertise: Argus Safety, Axway Gateway, Apex, BI Publisher. · ...

The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. · ...

Manage guest posting and article submissions as well as blog network submissions. · ...

Job Title: · Regulatory Submissions Associate - ICSR & Aggregate · Location: · Remote / Bangalore · Experience: · 3–5 Years · Employment Type: · Full-time · Role · We are looking for a Regulatory Affairs Associate with solid experience in · ICSR submissions and Aggregate Safety R ...

As a Digital Content Writer at Pereyan you will be responsible for creating engaging and informative content for various platforms. · ...

We have an exciting role MLR Submission – Analyst to head our creative studio for one of Omnicom's largest advertising agencies. · This leadership role will require leading and drive world-class advertising, creative and studio deliverables working with global brands and agency l ...

Attend Daily Monitoring meeting & Escalation of Open Point ECI Management activities Claim cost communication to customer Customer schedule follow up & Communication to PC - OE - SP RDDP & ECI Upload ASA DCS Drawing submission to customer Sharing RDDP & Drawing submission to cust ...

You will be responsible for managing and overseeing end-to-end content submission processes while ensuring submissions are timely, accurate, and compliant with given Brand/AMA guidelines. · This role entails conducting quality control checks, including proofreading and fact-check ...

We are looking for an experienced Technical Support Specialist with strong expertise in pharmacovigilance (PV) systems. · Argus System Management: Configure Argus PLS, reporting rules and system settings. · Maintain Axway Gateway connections and perform certificate updates. · ...