Quality Coordinator for New Product Introduction Department
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Are you motivated by working with quality of drug product processes? Do you always strive for setting the right level of quality standards, and get energy from working and sparring with a wide range of highly qualified colleagues ?
Then you might be the future Quality Coordinator we are looking for to join us in New Product Introduction!
The position
As department Quality Coordinator, you will work closely with our Management Group, and be responsible for supporting the department and colleagues in maintaining and striving for high quality level in our processes. Your tasks will include,
Your job will be characterized by a dynamic mix of coordination within and outside the department, assisting your colleagues and management, follow-up and participation in management related activities, and execution of your own tasks. Therefore, you must have and be motivated by a flexible workstyle and ability to prioritize your own tasks and time.
Qualifications
To be successful in the role we expect you to have:
You are positive, cooperative and solution oriented, and you work systematically, logically, and proactively. You are comfortable speaking your mind, and to communicate at all levels of the organisation. You take pride in solving your tasks as close to the process as possible and with close involvement of your key stakeholders. You take initiatives on your own, and you ensure commitment from your stakeholders.
About the department
New Product introduction (NPI) is a part of Injectable Finished Products (IFP), Manufacturing Development, and consists of approximately 65 employees divided between 5 teams located in Bagsværd, DK . The main responsibility of NPI is the transition of development drug products into large scale production. This includes process design, material and process sciences, product stability, and coordination of production for late-phase clinical trials.
In the role as Quality Coordinator, you will organisationally be placed in the NPI Project Office together with the Project Managers who also work across teams in the department. The team consists of 8 Project Managers.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. 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 Director Charlotte Rossmeisl (+45 3075 9501)
Deadline
11th of December 2022. Applications and interviews will be screened and held on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV . To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
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Then you might be the future Quality Coordinator we are looking for to join us in New Product Introduction!
The position
As department Quality Coordinator, you will work closely with our Management Group, and be responsible for supporting the department and colleagues in maintaining and striving for high quality level in our processes. Your tasks will include,
- Coach and assist your colleagues in GxP related tasks such as deviations and changes
- Drive preparation for and follow up on internal audits and authority inspections
- Maintain a quality overview and assist the department reporting on GMP and quality trends
Your job will be characterized by a dynamic mix of coordination within and outside the department, assisting your colleagues and management, follow-up and participation in management related activities, and execution of your own tasks. Therefore, you must have and be motivated by a flexible workstyle and ability to prioritize your own tasks and time.
Qualifications
To be successful in the role we expect you to have:
- A M.Sc . or B.Sc . within Engineering, Chemistry, Biophysics, or other relevant scientific discipline, alternatively you have a lab technician education
- 2-4 years of experience from pharmaceutical or medical device industry
- Experience with complex processes and with GMP regulated areas
- Fluency in English verbally and in writing
You are positive, cooperative and solution oriented, and you work systematically, logically, and proactively. You are comfortable speaking your mind, and to communicate at all levels of the organisation. You take pride in solving your tasks as close to the process as possible and with close involvement of your key stakeholders. You take initiatives on your own, and you ensure commitment from your stakeholders.
About the department
New Product introduction (NPI) is a part of Injectable Finished Products (IFP), Manufacturing Development, and consists of approximately 65 employees divided between 5 teams located in Bagsværd, DK . The main responsibility of NPI is the transition of development drug products into large scale production. This includes process design, material and process sciences, product stability, and coordination of production for late-phase clinical trials.
In the role as Quality Coordinator, you will organisationally be placed in the NPI Project Office together with the Project Managers who also work across teams in the department. The team consists of 8 Project Managers.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. 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 Director Charlotte Rossmeisl (+45 3075 9501)
Deadline
11th of December 2022. Applications and interviews will be screened and held on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV . To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 17.11.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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