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
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,
Build our future together: Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines
Job Description SummaryWe are looking for an AI-enabled Scientific Computing Expert to strengthen Drug Product development capabilities within a global CMC organization. In this role, you will focus on how AI, data science, and modeling can improve decision-making
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
Role Purpose Lead end-to-end Injectable (Drug- Device Combination) development programs across R&D, Clinical, Regulatory, and Manufacturing. Ensure delivery aligned to cost, timelines, and global regulatory expectations for advanced markets. Key Accountabilities 1. Program Governance & Execution -
Position Overview: The Business Development Manager (BDM) will be responsible for driving business growth specifically for Natural Marble division. This individual will work closely with Architects, Interior Designers (also if required with Contractors). As a key player
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
Career CategoryInformation Systems Job Description Job Description 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, develop, manufacture and
JOB TITLE Assistant Manager I, Quality Compliance JOB PURPOSE Generic Implement Quality Compliance & Regulatory Affairs activities at Ankleshwar site adhering to Zentiva Corporate Quality Policies, Regulatory and HSE guidelines with optimum utilization of resources to
Department: Validation COE Company: Novo Nordisk Global Business Services (GBS) Help safeguard the systems that keep patient safety at the heart of everything we do. If you thrive at the intersection of compliance, technology and collaboration
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismData, Analytics & AI Management LevelAssociate Job Description & SummaryAt PwC, our people in business application consulting specialise in consulting services for a variety of business applications, helping clients optimise operational
Regulatory Consultant 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 complexity, anticipate change
Work ScheduleSecond Shift (Afternoons) Environmental ConditionsOffice Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission
At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated
Build our future together: Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines
Lifecycle & Channel Marketing Specialist (Aftermarket & Partner Growth) Location: New Delhi, India (Work from Office) About Us: Ingersoll Rand is a global industrial leader known for delivering innovative and mission-critical technologies across air, fluid, energy,
Company: Novo Nordisk Global Business Services (GBS) Bring life-changing medical devices and combination products to patients faster. In this role, youll act as a true ambassador for our device portfolio – shaping regulatory strategy, engaging with
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