Sr. Regulatory Publishing Specialist

Sr Manager - Gen Med Biosims International Regulatory LeadThe Senior Manager of Regulatory Affairs at Amgen oversees regulatory compliance initiatives within the company. They are responsible for ensuring all company procedures and products adhere to state and federal regulatory requirements.Group PurposeInternational Regulatory Affairs provides...

Company DescriptionDyaz Innovate is a software company with its flagship product, DyazRIMS, which supports the entire regulatory compliance process. The company is committed to enhancing regulatory processes for clients globally and promotes an engaging and supportive work environment.Role DescriptionThis is a full-timeon-siterole for a Senior Regulatory...

The International Regulatory Lead (IRL) Sr Associate will provide coordination and execution of regulatory deliverables for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams toOptimize product development and regulatory approvals in International countriesDevelop...

Job Description:Sr. Specialist - CyberArkWe are seeking a skilled CyberArk Technical Specialist. The ideal candidate will be responsible for managing and maintaining the CyberArk privileged access security platform. This includes ensuring its continuous improvements and providing technical inputs and optimization to the existing environment. The Sr...

OverviewVelocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We...

Career CategoryRegulatoryJob DescriptionABOUT AMGENAmgen 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 deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeRegulatory Affairs Specialist In this exciting role as a Regulatory Affair Specialist, you will...

We are seeking a highly organized and detail-orientedRegulatory Project Coordinator/Managerto be the central point of contact between our Head Office (HO) and our Emerging Market country teams. This critical role ensures the seamless and timely delivery of all regulatory, technical, and administrative documentation required for product registration, dossier...

Role & responsibilitiesCMC and Labelling:Preparation of ANDAs in eCTD format for various type of formulationsReview of the technical documents such as Specifications, BMR, MFC,Able to work on All type of CTD section write-upsHands on experience on life cycle management activity (AR, CBE, CBE-30 and PAS)Through knowledge on ICH guidancesShould able to handle...

One of my direct clients in Hyderabad is looking for the following: this would be a hybrid opportunity.Long Term Contract Opportunity:Full-Time ContractorRole: Sr Oracle EDI/EBS SpecialistLocation: Nanakramguda, HyderabadHybrid Model- 3Days weekly from the officeImmediate JoinerTimings: 10-5 PM IST Monday to FridaySalary: Best Per MonthClient is performing a...