Regulatory Professional I

Department: RA Labelling Projects & Planning Are you detail-oriented and passionate about ensuring regulatory compliance? Do you thrive in a fast-paced and global environment? We are looking for a Regulatory Professional I - Labelling to join our team in Global Business Services (GBS) Bangalore. If you are ready for a challenging role where you can...

The position As a Regulatory Professional I - Labelling at Novo Nordisk, you will be responsible for the following: Packaging Material Coordination: Collaborate with stakeholders across Regulatory Affairs, Affiliate, Product Supply, and Marketing to plan and coordinate packaging material for global markets. Labelling Request Management: Assess and...

Job Title: Regulatory Affairs Manager I Career Level - D Introduction to role: Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management capabilities to lead the end-to-end planning, coordination, and execution of assigned deliverables. You...

Department: Labelling Operations Are you skilled in graphic design and have experience in regulatory affairs? Are you ready for the next step in your career? We are looking for a Regulatory Professional II to join our Global Regulatory Affairs team in Novo Nordisk. If you have a passion for design and ensuring regulatory compliance, read on and...

    Department: Regulatory Affairs Rare Endocrine Disorders   Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and ensuring Novo Nordisk’s license to operate by supporting in creating regulatory strategies? We...

Department: Labelling Designers Are you a regulatory professional looking for an exciting opportunity in the pharmaceutical industry? Do you have experience in labelling and a passion for ensuring high-quality product approvals? Join our team at Novo Nordisk as an RA Labelling professional and make a difference in the lives of millions of patients...

    Department: EU Submissions Hub   Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to...

Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic...

The position As a RA Specialist, the ideal candidate will be responsible to design RA Strategy from late stage development and throughout Life cycle of the device project, prepare and submit high quality files to the authorities achieving fast approvals. Act as an ambassador for assigned medical devices/device part of combination products. This...

Department: Regulatory Affairs Rare Endocrine Disorders Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and ensuring Novo Nordisk’s license to operate by supporting in creating regulatory strategies? We...

Department: EU Submissions Hub Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to...

Job Summary: As a Claims Specialist I at Chase, you will focus on delivering business results, providing unique solutions to customers, and showcasing your communication, negotiation, and decision-making skills. You will be required to demonstrate resilience and adaptability in a fast-paced environment, navigate multiple technologies, and adhere to...

Job TitleSecurity specialist - Regulatory & StandardsJob DescriptionJob title:Security specialist - Regulatory & StandardsYour role:As the Product Security process expert you will responsible for maintaining and enhancing the global Philips Product Security policy and process framework, driving the future strategic directions on product security...

Department: Regulatory Affairs Rare Endocrine Disorders Job Level: 7 Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and ensuring Novo Nordisk’s license to operate by supporting in creating regulatory...

We’re looking for people who are determined to make life better for people around the world. Purpose: Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across...

Description The Regulatory Affairs Manager 1 with Business Development role sits in the Regulatory Business Development group and is of key importance in the delivery of AstraZeneca business development portfolio to ensure license transition in the most efficient and customer focused manner. The role comprises of two main accountabilities,...

Description The Regulatory Affairs Manager 1 with Business Development role sits in the Regulatory Business Development group and is of key importance in the delivery of AstraZeneca business development portfolio to ensure license transition in the most efficient and customer focused manner. The role comprises of two main accountabilities, described...

Department: Novo Nordisk Quality Global Business Solution Are you passionate about ensuring quality standards and compliance? Do you have experience in approval of Master data in SAP? We are looking for a Senior Quality Professional to join our team at Novo Nordisk. If you are ready for a new challenge and want to make a difference in the...

Key Responsibilities : Accountable to the GRL and Global Regulatory staff for the delivery of Marketing Application, pre-approval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines and in line with GSK SOPs and working practices May be responsible for...

    Department: Novo Nordisk Quality Global Business Solution   Are you passionate about ensuring quality standards and compliance? Do you have experience in approval of Master data in SAP? We are looking for a Senior Quality Professional to join our team at Novo Nordisk. If you are ready for a new challenge and want to make a difference in the...