QA for Innovation Project
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In Novo Nordisk IFP, we are on a continuous journey to innovate and bring in new technical solutions to our aseptic process. We are looking for a QA to take part in this as project QA, and ensure that quality is build into innovation projects from start to finish. Does this sound like a role for you? Then you might be the person we are looking for in QA for IFP ManDev (Injectable Finished Products, Manufacturing Development). The position
As project QA, you will ensure that projects have early Q involvement and set the right balanced quality levels, to ensure that we continue to deliver high quality processes. The innovation and technology projects are focused on aseptic production lines, and surrounding processes. Focus of the projects, is to increase effectiveness, simplify or ensure regulatory compliance. Alongside working with projects, this role also includes review and approval of documents within our area of responsibility, “products” and “processes” for aseptic manufacturing. Within this responsibility we ensure that quality and compliance is upheld for all drug product sites producing diabetes and obesity products. We set direction and approve documents within ex. product specifications, compatibility of process aids and primary packaging and stability studies.
To succeed in this role, you will use your strong communication and social skills, to set quality direction for stakeholders and be a present character on the shopfloor. The role requires proactive oversight and the will to identify and ensure improvements for the area.
We offer you an exciting, challenging, and important role where you become part of a skilled team which acts as quality sparring partners for our stakeholders, both locally and internationally. You will get great opportunities for both personal and professional development, with growing responsibility depending on your skills and interests.
Qualifications
• Master’s degree in Engineering, Biology, Chemistry, Pharmacy, or similar
• Solid GMP experience from pharmaceutical industry.
• Experience with project work.
• Being a self-driven, proactive, and resourceful person
• Ability to set the right and balanced quality standards and ensure compliance within regulatory requirements
• Thriving in a dynamic environment where collaboration and communication with many different stakeholders will be crucial for your success
About the department
You will become part of a great department with many interfaces around the organisation, both in Denmark and our international production sites. The department consists of 40 people divided into three teams, “Products & Processes”, “QC” and “Support”. The department consists of highly knowledgeable and skilled people, covering the diverse area of ManDev.
In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective.
Working at Novo Nordisk
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. Novo Nordisk provides various opportunities for professional growth and impactful achievements. You will get a range of possibilities and chances to work in an exciting growth journey within Fill & Finish Project QA, ensuring the quality and safety of products. As a senior QA Professional, you will have the chance to develop competencies that can help develop and broaden your knowledge and skills and make a significant impact on the organization.
Contact
For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594.
Deadline
2nd of October 2023.
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.
As project QA, you will ensure that projects have early Q involvement and set the right balanced quality levels, to ensure that we continue to deliver high quality processes. The innovation and technology projects are focused on aseptic production lines, and surrounding processes. Focus of the projects, is to increase effectiveness, simplify or ensure regulatory compliance. Alongside working with projects, this role also includes review and approval of documents within our area of responsibility, “products” and “processes” for aseptic manufacturing. Within this responsibility we ensure that quality and compliance is upheld for all drug product sites producing diabetes and obesity products. We set direction and approve documents within ex. product specifications, compatibility of process aids and primary packaging and stability studies.
To succeed in this role, you will use your strong communication and social skills, to set quality direction for stakeholders and be a present character on the shopfloor. The role requires proactive oversight and the will to identify and ensure improvements for the area.
We offer you an exciting, challenging, and important role where you become part of a skilled team which acts as quality sparring partners for our stakeholders, both locally and internationally. You will get great opportunities for both personal and professional development, with growing responsibility depending on your skills and interests.
Qualifications
• Master’s degree in Engineering, Biology, Chemistry, Pharmacy, or similar
• Solid GMP experience from pharmaceutical industry.
• Experience with project work.
• Being a self-driven, proactive, and resourceful person
• Ability to set the right and balanced quality standards and ensure compliance within regulatory requirements
• Thriving in a dynamic environment where collaboration and communication with many different stakeholders will be crucial for your success
About the department
You will become part of a great department with many interfaces around the organisation, both in Denmark and our international production sites. The department consists of 40 people divided into three teams, “Products & Processes”, “QC” and “Support”. The department consists of highly knowledgeable and skilled people, covering the diverse area of ManDev.
In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective.
Working at Novo Nordisk
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. Novo Nordisk provides various opportunities for professional growth and impactful achievements. You will get a range of possibilities and chances to work in an exciting growth journey within Fill & Finish Project QA, ensuring the quality and safety of products. As a senior QA Professional, you will have the chance to develop competencies that can help develop and broaden your knowledge and skills and make a significant impact on the organization.
Contact
For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594.
Deadline
2nd of October 2023.
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.
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 24.7.2023, 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.
- Øvrige
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