Company: Novo Nordisk Global Business Services (GBS) Shape regulatory strategies that bring life-changing medicines from development through approval – and into the hands of patients across the globe. Your new role As a CMC Regulatory Specialist, you will
Description: This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across various dosage forms, with a specific focus on inhalation
Regulatory Consultant (CMC-EU, GCC & AU) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate
Description: Key Responsibilities Lead the development, organization, and maintenance of Design History File (DHF) documentation in compliance with 21 CFR 820.30, combination product requirements, and internal procedures Author and technically own key design control deliverables, including design
Key Responsibilities Lead the Device Development department in Amneal India R&D settings Manage direct reportee(s) Lead the development, organization, and maintenance of Design History File (DHF) documentation in compliance with 21 CFR 820.30, combination product requirements, and internal
Job Title: R&D GRA CMC Team Lead Location: Hyderabad (Hybrid) Level: L3-2 About the job Our Team: The Global Regulatory Affairs (GRA) CMC & Device Organization serves as a critical strategic partner within Sanofis regulatory framework, providing expert
Job title: R&D GRA CMC Lead Location: Hyderabad About the job Our Team: The Global Regulatory Affairs (GRA) CMC & Device Organization serves as a critical strategic partner within Sanofis regulatory framework, providing expert guidance on Chemistry, Manufacturing,
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
The Business Development Manager will be responsible for driving commercial growth of CDMO and regulatory services by developing new business opportunities, managing client relationships, and expanding the company’s presence across global pharmaceutical and biotech markets. This role
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Department: Global Supply Chain Design Organization: Novo Nordisk Global Business Services (GBS) India Drive data excellence that ensures life-saving medicines reach patients on time, every time. Your new role As a Associate Master Data Professional I,
Job Description Summary#LI-Hybrid Location: Hyderabad, India About this Role: As Manager, Competitive Intelligence (CI), Technical Research & Development (TRD), you will play a key role in establishing and driving the TRD Competitive Intelligence framework to support innovation,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of
Company: Novo Nordisk Global Business Services (GBS) Shape global regulatory strategies that bring innovative therapies from pipeline to patients – navigating complex health authority landscapes across the world while driving the future of how we work
We are Reckitt Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Key Responsibilities 1. Dossier Preparation & Submissions Prepare, review, and submit CTD / ACTD / country‑specific dossiers for: New product registrations Line extensions (strength, pack size, shelf life) Variations and renewals Coordinate compilation of Modules 1–5
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismData, Analytics & AI Management LevelManager Job Description & SummaryAt PwC, our people in data and analytics focus on leveraging data to drive insights and make informed business decisions. They utilise
Career CategoryInformation Systems Job Description Position Summary Amgens Drug Substance Technologies - Synthetics (DSTS) organization within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies that advance Amgens portfolio