Job Description

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 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

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