Regulatory Affairs Manager I

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: 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...

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 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...

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...

Job Description You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research.  Office-based in Bangalore Oversee preparation of clinical trial submission...

Job DescriptionYou will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research.  Office-based in Bangalore Oversee preparation of clinical trial submission dossiers for...

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 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...

Position: Manager - Public AffairsLocation: BangaloreJob Responsibility:The role will be responsible for managing Xiaomi's reputation in the Government and amongst Industry stakeholders and executing various initiatives to for stakeholder management and confidence building. The role operates at the intersection of Policy advocacy, Corporate PR and...

Position: Manager Public AffairsLocation: BangaloreJob Responsibility:The role will be responsible for managing Xiaomi's reputation in the Government and amongst Industry stakeholders and executing various initiatives to for stakeholder management and confidence building. The role operates at the intersection of Policy advocacy, Corporate PR and...

When our values align, there's no limit to what we can achieve.   Job Description: Relevant experience in regulatory package preparation, compilation and submission to Health Authorities in various markets  with focus on EU countries . Working knowledge of EU regulatory procedures including adaptability to strict Health Authority and Sponsor...

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...

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...

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...

    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...

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

Are you interested in a highly visible, global role that allows you to lead a team of regulatory experts while being part of the CMC regulatory leadership team to contribute to the advancement of a robust and innovative product pipeline? If so, this role is an exciting move to explore. GSK has a large, well established and largely in-commercial-supply...

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...