Novo Nordisk Regulatory Project Manager Job Opening, Apply Now
Regulatory Project Manager
Category: Reg Affairs & Safety Pharmacovigilance
Location: Bangalore, Karnataka, IN
Department: International Operations Regulatory Affairs Bangalore
Are you experienced in project management? Do you thrive in a fast-paced and dynamic environment? We are looking for a Regulatory Project Manager to join our IO Regulatory Affairs team in Bangalore. If you are passionate about ensuring compliance and driving successful projects, read on and apply today for a life-changing career.
The Position
As a Regulatory Project Manager at Novo Nordisk, you will:
- Timely plan and execute regulatory projects based on identified needs and objectives.
- Manage working relationships with key internal and external stakeholders.
- Engage with vendors, evaluate proposals, and manage risks during project execution.
- Enable digital solutions to address issues in systems like Veeva Vault etc.,
- Organize and manage regulatory project-related events in the International Operations (IO) region, fostering stakeholder participation and collaboration.
Qualifications
To be successful in this role, we are looking for someone with the following qualifications:
- Graduate/Postgraduate degree in Science, Pharmacy, Medicine, or related fields.
- 6+ years of work experience within relevant qualifiers as listed below.
- Strong strategy development and analytical skills, coupled with a deep understanding of Regulatory Affairs operations at country or regional levels.
- Proven track record in planning and executing projects within mature organizations.
- Experience in driving change management initiatives; possession of a project management certification is preferred.
- Fluent in written and spoken English, proficient in MS Office, and excellent communication and negotiation skills.
About the Department
The IO Regulatory Affairs department is responsible for ensuring regulatory compliance for new products and product amendments. We work closely with health authorities and policymakers to shape future regulatory frameworks. Our team also focuses on product safety through safety pharmacovigilance, ensuring medicines are safe to use. We collect, analyze, and report safety data, and continuously monitor for new safety signals. Join our team in Bangalore and contribute to our mission of safeguarding patients and expanding the availability of life-changing products.
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 application tool.
Deadline
Apply on or before 14th June 2024.
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