Development QA engineer
- Quality
- Denmark - Hillerød
Would you like to help securing Novo Nordisk A/S portfolio of prefilled devices continuously is improved to the benefit of our customers? Do you get energized by working in a project team and handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD), Prefilled QA.
About the department
DMD Prefilled QA is responsible for quality assurance activities within the prefilled device area from early device development projects throughout the entire life cycle of the products.
You will become part of a department with 15 highly skilled and motivated QA employees, and you will together with some of your QA colleagues be based in Device R&D as part of the cross functional project teams managed by Device R&D project managers.
The job
In DMD prefilled QA, we are seeking a dynamic, committed employee who wants to proactively influence the quality of our future prefilled devices.
You will, together with your colleagues, be responsible for quality assurance activities such as support, review and approval of documentation in device development projects. This also includes responsibility for quality specifications, input to the risk management process, design verification and validation as well as other design control activities.
Your stakeholder portfolio is wide and your results are highly dependent on cooperation and communications skills and your ability to take initiatives.
Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements.
You are familiar working in a team and used to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energized by learning new things. You are robust, can keep focus and you have good communication skills. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call Inger Sorensen on + 45 3075 4648.
Deadline
23 August 2013.
- Quality
- Denmark - Hillerød
Would you like to help securing Novo Nordisk A/S portfolio of prefilled devices continuously is improved to the benefit of our customers? Do you get energized by working in a project team and handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD), Prefilled QA.
About the department
DMD Prefilled QA is responsible for quality assurance activities within the prefilled device area from early device development projects throughout the entire life cycle of the products.
You will become part of a department with 15 highly skilled and motivated QA employees, and you will together with some of your QA colleagues be based in Device R&D as part of the cross functional project teams managed by Device R&D project managers.
The job
In DMD prefilled QA, we are seeking a dynamic, committed employee who wants to proactively influence the quality of our future prefilled devices.
You will, together with your colleagues, be responsible for quality assurance activities such as support, review and approval of documentation in device development projects. This also includes responsibility for quality specifications, input to the risk management process, design verification and validation as well as other design control activities.
Your stakeholder portfolio is wide and your results are highly dependent on cooperation and communications skills and your ability to take initiatives.
Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements.
You are familiar working in a team and used to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energized by learning new things. You are robust, can keep focus and you have good communication skills. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call Inger Sorensen on + 45 3075 4648.
Deadline
23 August 2013.