Senior QA Professional
- Research & Development
- Denmark - Gentofte
Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Professional in a job that includes many different clinical stages of the product development.
About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredients (API) activity in our development and support projects live up to the cGMP requirements.
We are 29 colleagues in two teams. You will join the Process Compliance team and have 10 dedicated colleagues. Our mission is to assure that our pilot plants (cell banks, cell cultivation, purification and chemical synthesis) and development laboratories meet the internal and external requirements. The pilot plants and the development laboratories are located in Bagsværd, Gentofte, Måløv and Hillerød, and you will move between the different locations and the QA office on a day-to-day basis.
The job
You assure best-in-class quality of our production areas regarding validation and qualification of the equipment, environment and utilities. Document approval in connection with qualification, cleaning, maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in investment projects, rebuilding of existing facilities and building of new facilities. In close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for our pilot plants.
We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.
Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 6 years’ experience with GMP, equipment/facilitation, qualification and cleaning from the QA area. As we operate in an international environment, you must speak and write English fluently.
You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.
At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines.
Contact
For further information, please contact Lisbeth Voetmann +45 3075 0530 or Peter Søtofte Elten at +45 3079 8453.
Deadline
4 August 2013.
- Research & Development
- Denmark - Gentofte
Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Professional in a job that includes many different clinical stages of the product development.
About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredients (API) activity in our development and support projects live up to the cGMP requirements.
We are 29 colleagues in two teams. You will join the Process Compliance team and have 10 dedicated colleagues. Our mission is to assure that our pilot plants (cell banks, cell cultivation, purification and chemical synthesis) and development laboratories meet the internal and external requirements. The pilot plants and the development laboratories are located in Bagsværd, Gentofte, Måløv and Hillerød, and you will move between the different locations and the QA office on a day-to-day basis.
The job
You assure best-in-class quality of our production areas regarding validation and qualification of the equipment, environment and utilities. Document approval in connection with qualification, cleaning, maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in investment projects, rebuilding of existing facilities and building of new facilities. In close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for our pilot plants.
We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.
Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 6 years’ experience with GMP, equipment/facilitation, qualification and cleaning from the QA area. As we operate in an international environment, you must speak and write English fluently.
You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.
At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines.
Contact
For further information, please contact Lisbeth Voetmann +45 3075 0530 or Peter Søtofte Elten at +45 3079 8453.
Deadline
4 August 2013.