QA Professional
- Quality
- Denmark - Måløv
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 Academic 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 Ingredient (API) activity in our development and support projects live up to the cGMP requirements.
We are 29 colleagues in three teams. You will join the Materials team and have 4 dedicated colleagues. Our job is to ensure product quality of incoming materials and the quality management system for this process.
The job
You assure best-in-class quality products from our suppliers. You will support our pilot facilities to have an overview of the complete supply chain from the materials going in to our clinical products. You will evaluate and implement new requirements in the department and the CMC supply area (app. 1000 people).
Other task will be release of materials, document approval in connection with Change request of any kind, e.g. new material, change to a material, change to our standard operating procedures.
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 Science, Chemical Engineering, Pharmaceutical Sciences or possess equivalent qualifications besides a strong quality mind-set. You have at least 3 years’ experience with GMP, product release, production or quality assurance. As we operate in both a national and international environment, you must speak and write English fluently. We have a lot of IT-systems to handle our materials, e.g. SAP and LIMS. Therefore you need to have a flair for IT – systems.
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.
You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. You have focus on results and quality – and contribute to the right level of compliance.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Peter Søtofte Elten at +45 3079 8453.
Deadline
27 November 2013
- Quality
- Denmark - Måløv
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 Academic 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 Ingredient (API) activity in our development and support projects live up to the cGMP requirements.
We are 29 colleagues in three teams. You will join the Materials team and have 4 dedicated colleagues. Our job is to ensure product quality of incoming materials and the quality management system for this process.
The job
You assure best-in-class quality products from our suppliers. You will support our pilot facilities to have an overview of the complete supply chain from the materials going in to our clinical products. You will evaluate and implement new requirements in the department and the CMC supply area (app. 1000 people).
Other task will be release of materials, document approval in connection with Change request of any kind, e.g. new material, change to a material, change to our standard operating procedures.
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 Science, Chemical Engineering, Pharmaceutical Sciences or possess equivalent qualifications besides a strong quality mind-set. You have at least 3 years’ experience with GMP, product release, production or quality assurance. As we operate in both a national and international environment, you must speak and write English fluently. We have a lot of IT-systems to handle our materials, e.g. SAP and LIMS. Therefore you need to have a flair for IT – systems.
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.
You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. You have focus on results and quality – and contribute to the right level of compliance.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Peter Søtofte Elten at +45 3079 8453.
Deadline
27 November 2013