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
NetSuite CMC Consultant1 We are currently seeking an experienced NetSuite EPM Close Management & Consolidation Consultant to support the implementation and optimization of NetSuite EPM. This role will be key in designing and deploying Close Management and
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and
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Job Title: International CMC Regulatory Affairs Manager I Global Career Level: D Role Type: Individual Contributor for International Markets About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization
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
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
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,
Career CategoryRegulatory Job Description Job Description: Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the
Career CategorySupply Chain Job Description Manager, Product Lifecycle Management Execution ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover,
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science
Clinical Research and regulatory documentation Domain Expertise Regulatory submission expertise across CTD/eCTD formats — deep familiarity with the Common Technical Document structure (Modules 1–5) and how CMC (Module 3), nonclinical/toxicology (Module 4), and clinical (Module 5) sections
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Manager Qualifications:MSc Years of Experience:13 to 18 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud
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
Job Description Primary Job Responsibilities: Product characterization using LC/MS for biosimilarity studies. Training related to advanced LC-MS applications and DQA SOPs. Planning of experiments. Drafting and/or review reports and presentations on experimental data and scientific outcomes
Founded in 1991, Mindray is one of the leading global providers of medical devices and solutions. Firmly committed to our mission of “advance medical technologies to make healthcare more accessible”, we are dedicated to innovation in
Regulatory Affairs Specialist Location: Hyderabad, India (Hybrid) *Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza’s Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory submissions.
Regulatory Affairs Senior Specialist Location: Hyderabad, India (Hybrid) *Relocation assistance is available for eligible candidates and their families, if needed Join Lonza’s Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory