Job Description
Manager of RA Established Products
The department is currently being established and will be handling regulatory clinical activities within the established product portfolios.
The position holder will have a dotted line to CVP of RA Diabetes and Obesity and CVP of Biopharm in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
Manager of RA Established Products
The department is currently being established and will be handling regulatory clinical activities within the established product portfolios.
The position holder will have a dotted line to CVP of RA Diabetes and Obesity and CVP of Biopharm in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
Manager of RA Established Products, CMC & Devices 1
The department is currently responsible for all regulatory CMC and device aspects of the HRT (hormone replacement therapy) portfolio, glucagon portfolio and growth hormone portfolio in addition to a several device products. The position holder will have a dotted line to VP of RA CMC & Devices in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
The department is currently responsible for all regulatory CMC and device aspects of the HRT (hormone replacement therapy) portfolio, glucagon portfolio and growth hormone portfolio in addition to a several device products. The position holder will have a dotted line to VP of RA CMC & Devices in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
Manager of RA Established Products, CMC & Devices 2
The department is currently being established and responsibilities within the established product portfolios will transition from the Denmark unit to this team
The position will have a dotted line to VP of RA CMC & Devices in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
The department is currently being established and responsibilities within the established product portfolios will transition from the Denmark unit to this team
The position will have a dotted line to VP of RA CMC & Devices in Denmark and in this way ensure functional alignment across the products and projects handled by the different departments.
As the Bangalore unit is expanding, these positions will play a key role in building strong teams and in strengthening the collaboration across the Global Regulatory Affairs organisation. While building the teams it will be critical to ensure people development and maintain high engagement in the teams.
All positions present an opportunity to demonstrate strong leadership in accordance with the company charter, which we at Novo Nordisk call the Novo Nordisk WAY. We expect that each position holder will lead with a strong focus on continuous improvement, while ensuring a high-quality mind-set and adherence to Novo Nordisk quality management system. As a leader, you will be expected to ensure optimal and flexible use of resources within the department, while continuing to develop, coach and support employees to achieve higher levels of professional competency for current and future roles.
Candidate Profile
You hold a Master of Science or other relevant Professional Degree (e.g. MD, PhD) combined with 5+ years’ experience from the pharmaceutical industry, preferably within global regulatory affairs organisation with project-based tasks.
You have strong people management skills, efficient negotiator and have good stakeholder management skills and lead by example and set direction. Furthermore, you motivate employees and keep engagement high in your department. You are flexible, quick to adapt and able to handle many responsibilities, while delivering results - Proactive and solution oriented. You hold good communication and presentation skills and is fluent in spoken and written English.
You hold a Master of Science or other relevant Professional Degree (e.g. MD, PhD) combined with 5+ years’ experience from the pharmaceutical industry, preferably within global regulatory affairs organisation with project-based tasks.
You have strong people management skills, efficient negotiator and have good stakeholder management skills and lead by example and set direction. Furthermore, you motivate employees and keep engagement high in your department. You are flexible, quick to adapt and able to handle many responsibilities, while delivering results - Proactive and solution oriented. You hold good communication and presentation skills and is fluent in spoken and written English.
Additional Information
Experience : 5+ years
Qualification : MD, Ph.D
Location : Karnataka - Bangalore
Industry Type : Pharma/ Healthcare
Functional Area : Regulatory Affairs
End Date : 15th December, 2018
Experience : 5+ years
Qualification : MD, Ph.D
Location : Karnataka - Bangalore
Industry Type : Pharma/ Healthcare
Functional Area : Regulatory Affairs
End Date : 15th December, 2018
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