Product Surveillance Advisor
- Quality
- Denmark - Bagsværd
This is a highly versatile job where you will gain broad exposure to the company through regular interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the globe. You will frequently report directly to top management where your written and presentation skills must be excellent. If you find this challenging and inspiring, then you might be our new colleague in Global Safety.
About the department
Handling potential recall situations and surveiling global customer complaint data are the responsibility of CCC in Global Safety. We are located in House of Quality in Bagsværd.
The Job
The job is a 12 month temporary position starting 1st of February 2014.
You will be responsible for the surveillance and trending of data generated by clinical trials and customer complaints and for managing product recall situations from clinical trials and on marketed products. Our department is responsible for detecting, investigating and reporting complaint trends to top management and management forums. In product recall situations, you will be responsible for coordinating all relevant investigations and will handle the contact with regulatory authorities such as the FDA and EMA. We are also represented in various committees, e.g. safety committees and complaint surveillance groups where we provide input to local management, Product Supply and R&D.
Therefore, you will get the opportunity to work broadly within Novo Nordisk connecting with R&D, production sites, marketing departments and several of our international affiliates. In CCC, we work at the interface of our products and the patients and are responsible for maximizing the value of patient feedback by capturing the data and incorporating it back into Novo Nordisk processes.
Qualifications
You hold an academic degree in pharmaceutical sciences, engineering or a related natural science discipline and you have a strong quality mindset.
The ideal candidate has experience from CMC supply, Product Supply, QC, QA, Regulatory affairs or health authorities. Your analytical skills are excellent, and you can navigate in an organization under difficult circumstances and ensure a high level of communication. In your previous assignments you have demonstrated solid skills in writing reports and making presentations.
You are a positive and open minded team player who can co-operate at all organizational levels. You like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines and meeting business targets.
Strong communication skills are required, so it is expected that you are fluent in English, both written and spoken.
We offer a very exciting job amongst good colleagues with diverse backgrounds in a positive working environment.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Lisbet Bærentzen at +45 3079 8080.
Deadline
15th of December 2013
- Quality
- Denmark - Bagsværd
This is a highly versatile job where you will gain broad exposure to the company through regular interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the globe. You will frequently report directly to top management where your written and presentation skills must be excellent. If you find this challenging and inspiring, then you might be our new colleague in Global Safety.
About the department
Handling potential recall situations and surveiling global customer complaint data are the responsibility of CCC in Global Safety. We are located in House of Quality in Bagsværd.
The Job
The job is a 12 month temporary position starting 1st of February 2014.
You will be responsible for the surveillance and trending of data generated by clinical trials and customer complaints and for managing product recall situations from clinical trials and on marketed products. Our department is responsible for detecting, investigating and reporting complaint trends to top management and management forums. In product recall situations, you will be responsible for coordinating all relevant investigations and will handle the contact with regulatory authorities such as the FDA and EMA. We are also represented in various committees, e.g. safety committees and complaint surveillance groups where we provide input to local management, Product Supply and R&D.
Therefore, you will get the opportunity to work broadly within Novo Nordisk connecting with R&D, production sites, marketing departments and several of our international affiliates. In CCC, we work at the interface of our products and the patients and are responsible for maximizing the value of patient feedback by capturing the data and incorporating it back into Novo Nordisk processes.
Qualifications
You hold an academic degree in pharmaceutical sciences, engineering or a related natural science discipline and you have a strong quality mindset.
The ideal candidate has experience from CMC supply, Product Supply, QC, QA, Regulatory affairs or health authorities. Your analytical skills are excellent, and you can navigate in an organization under difficult circumstances and ensure a high level of communication. In your previous assignments you have demonstrated solid skills in writing reports and making presentations.
You are a positive and open minded team player who can co-operate at all organizational levels. You like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines and meeting business targets.
Strong communication skills are required, so it is expected that you are fluent in English, both written and spoken.
We offer a very exciting job amongst good colleagues with diverse backgrounds in a positive working environment.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Lisbet Bærentzen at +45 3079 8080.
Deadline
15th of December 2013