Regulatory Specialist
2 weeks ago
Department : RA Labelling
Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials? Do you have expertise in labelling and project management? We are looking for a Regulatory Specialist to join our team in Bangalore and be part of our global Regulatory Affairs (RA) hub. If you are ready for a challenging and rewarding career, read on and apply today for a life-changing opportunity.
The position
As a Regulatory Specialist - Labelling, you will have the following responsibilities:
Set the regulatory strategy and plan, create, and drive projects to deliver high-quality global packaging materials.
Work as an integrated part of global cross-functional teams, collaborating with stakeholders ranging from labelling development to coordination with Novo Nordisk RA affiliates worldwide.
Plan and drive regulatory activities, including project management and adherence to agreed timelines and quality standards.
Demonstrate subject matter expertise in the labelling area and apply LEAN ways of working.
Qualifications
To be successful in this role, you should have the following qualifications:
Graduate/Postgraduate/ comparable degree in science-related field/packaging.
Minimum of 12-14 years of experience required in Project management/ Packaging/ Lean
Ability to successfully manage multiple projects, priorities, arrange and conduct meetings.
Adaptable and willing to learn new techniques.
Excellent communication and presentation skills.
Ability to cross collaborate and work with the teams and stakeholders from different backgrounds and culture in a Hybrid setup
It would be considered an advantage if you have:
Experience of leading projects through the full life cycle
Knowledge of Pharmaceutical Regulations and Guidelines
Global exposure in terms of handling different markets for pharmaceutical products
About the Department
The RA Labelling team in Bangalore is part of our global RA hub, consisting of four teams of high-caliber regulatory professionals and graphics designers. Our objective is to offer core Regulatory Affairs (RA) competencies to enable Novo Nordisk to secure fast, high-quality product approvals. We provide strategic and operational support on a global scale across the value chain, working closely with our colleagues in RAHQ, Denmark, and our affiliates worldwide.
Working at Novo Nordisk
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us Together, we go further. Together, we’re life changing.
Contact
If you believe you are a match for the above requirements and are willing to take up the role, please apply here with our online application tool.
Deadline
Apply on or before: 14th June 2024
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.
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