Senior Regulatory Professional
4 weeks ago
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 worldwide. Apply today for a life-changing career.
The Position
As a Senior Regulatory Professional, you are expected to demonstrate leadership quality by setting the regulatory strategy and being responsible for planning, creating, and submitting high-quality global packaging materials by using various graphic software to the health authorities, achieving fast approvals. You will work as an integrated part of global cross-functional teams with stakeholders ranging from labelling development, and labelling coordination to all Novo Nordisk RA affiliates worldwide.
As part of our department, you will be responsible for planning and driving regulatory activities and deliverables according to agreed timelines and quality. You must demonstrate subject matter expertise in Photoshop, InDesign, and Illustrator, along with knowledge of e-labelling.
Qualification
To be successful in this role, you should have:
Graduate/Postgraduate/comparable degree in graphical related field. Minimum of 10-12 years of graphical design experience is required. Proficiency in Adobe Photoshop, InDesign, and Illustrator. Good knowledge of Pantone and CMYK colours. Good knowledge of design guidelines, and style sheets. Ability to successfully manage multiple projects, and priorities, arrange and conduct meetings. PC illustration handling and colour separations. Adaptable and willing to learn new techniques. Excellent communication and presentation skills. Ability to cross-collaborate and work with teams and stakeholders from different backgrounds and cultures in a Hybrid setup.It would be considered an advantage if you have:
Experience in leading projects through the full life cycle. Knowledge of Pharmaceutical Regulations and Guidelines. Global exposure in terms of handling different markets for pharmaceutical products. Knowledge of e-labelling and hands-on experience with relevant applications like Adobe Dreamweaver with HTML, CSS, and JavaScript.About the Department
The RA Labelling team is part of Novo Nordisk Quality GBS, which was established in 2015. We are a global team of over 100 employees responsible for supporting and developing quality services for various units within Novo Nordisk. Our goal is to ensure high-quality and fit-for-purpose processes throughout the entire value chain. Join our ambitious and dynamic team and contribute to making quality easy, simple, and understandable.
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