Regulatory Professional I- Labelling Designer

10 hours ago

Bengaluru, India Novo Nordisk Full time

**Department: Global Regulatory Affairs - GBS**

**About the Department**

Global Regulatory Affairs (GRA) in Global Business Services (GBS) Bangalore is a global RA hub consisting of a strong team of high calibre regulatory professionals. The objective of the team is to offer core Regulatory Affairs (RA) competencies enabling NovoNordisk (NN) secure fast, high quality product approvals. The team delivers full strategic and operational support on a global scale across value chain on core regulatory processes across NN product portfolio. We provide regulatory expertise and work very closely with our colleagues in RAHQ, Denmark (DK) as well as colleagues in our affiliates all over the world.

**The Position**
- Conceptualize, design and develop outstanding creative based on written briefs that are given.
- Advanced understanding of design principles such as color, typography, layout, and information design
- Designing visual imagery for websites and ensuring in line with NN branding.
- Fluent with the Adobe suite - Photoshop (channels), Dreamweaver, InDesign, and Illustrator
- Communicating design ideas using user flows, process flows, site maps, and wireframes.

**Qualifications**:

- 5-8 years of experience along with Graduation and/or post-graduation/ comparable degree is required.
- Ability to successfully manage multiple projects and priorities since this is an individual contributor role.
- Proficiency in Adobe Photoshop, Dreamweaver, InDesign, and Illustrator.
- Project management skills are preferred.
- Excellent communication skills are expected.
- Good understanding on PC illustration handling and colour separations.
- Good understanding of content management systems.
- Excellent visual design skills.
- Adaptable and willing to learn new techniques.

**Working At Novo Nordisk**

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales
- we're all working to move the needle on patient care.

**Contact**

**Deadline**

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

  • Labelling Professional

    2 days ago

    Bengaluru, India Novo Nordisk Full time

    **Department: Labelling Projects & Planning** **About the Department** Global Regulatory Affairs (GRA) in Global Business Services (GBS) Bangalore is a global RA hub consisting of a strong team of high calibre regulatory professionals. The objective of the team is to offer core Regulatory Affairs (RA) competencies enabling NovoNordisk (NN) secure fast,...

  • Regulatory Professional I

    10 hours ago

    Bengaluru, India Novo Nordisk Full time

    **Department: International Operations Regulatory Affairs** **About the department** International Operations Regulatory Affairs Bangalore in Global Regulatory Affairs Global Business Services (GBS) is a global RA hub consisting of high calibre regulatory professionals. The objective of the team is to offer core RA competencies enabling NN secure fast,...

  • Labeling Designer

    4 weeks ago

    Bengaluru, India L&T Technology Services Full time

    Labeling DesignerExperience: 3-5yearsImmediate joiners preferredJob Description:- B.E. in Mechanical / Electrical / Electronic Engineering / MS in engineering preferred / Equivalent Degree- Work within labelling tools/systems to modify/create label templates- (FDA 21CFR Part 820, ISO 13485) Familiar with ISO 13485, ISO 15223, UDI, MDR, other applicable...

  • Regulatory Specialist III, Country Labelling

    3 weeks ago

    Bengaluru, India ScaleneWorks Full time

    Key Responsibilities ?: Author and compile Regional/Country PI as per regulatory authority labelling requirements and GSK process and standards. Author and compile market-specific supporting documentation for labelling submissions in accordance with regulatory authority requirements and GSK process and standards. Provide support to global and local GRA team...

  • Labeling Designer

    3 weeks ago

    Bengaluru, India L&T Technology Services Full time

    Labeling Designer Experience: 3-5years Immediate joiners preferred Job Description: B.E. in Mechanical / Electrical / Electronic Engineering / MS in engineering preferred / Equivalent Degree Work within labelling tools/systems to modify/create label templates (FDA 21CFR Part 820, ISO 13485) Familiar with ISO 13485, ISO 15223, UDI, MDR, other applicable...

  • Regulatory Professional I

    2 days ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Regulatory Professional I **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department: RA Submission Systems Development** - Are you passionate about ensuring compliance and streamlining regulatory processes in the dynamic field of life sciences? Do you have a passion for regulatory affairs and a desire to shape the...

  • Senior Regulatory Affairs Associate

    3 weeks ago

    Bengaluru, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Must have 4-6 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS,...

  • Regulatory Affairs Professional

    2 days ago

    Bengaluru, India Siemens Healthineers Full time

    o Supports worldwide product registrations by providing information and documents to Siemens Regional Unit (RU) in Asia-Pacific, Middle East Asia, South and Latin America and Europe. - o Provides answers to technical questions from Siemens Regional Unit (RU) and international regulatory authorities. - o Prepares and/or compiles technical documents for the...

  • labeling specialist

    3 weeks ago

    Bengaluru, India Biocon Biologics Full time

    Regulatory Affairs Labeling Specialist role Key Responsibilities:  Responsible for Creating Labeling Strategy for the health authority interactions and handling HA or Country Organization (CO) labeling queries for assigned program/ products.  Ensure Artwork Management for Initial Submission / Commercial Launch activities in coordination with CFT...

  • labeling specialist

    2 days ago

    Bengaluru, India Biocon Biologics Full time

    Regulatory Affairs Labeling Specialist roleKey Responsibilities: Responsible for Creating Labeling Strategy for the health authority interactions and handling HA or Country Organization (CO) labeling queries for assigned program/ products. Ensure Artwork Management for Initial Submission / Commercial Launch activities in coordination with CFT team....