Senior QA Professional
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Are you craving for an exciting job, where you will play a central role in securing the quality and safety of products for treating diabetes and obesity? Are you ready to be a part of a strong, fast moving, and evolving organisation?
If so, you may be the person we are looking for to support our Quality Assurance (QA) unit for Injectable Finished Products Manufacturing Development (IFP ManDev). Read more below and apply now for a life-changing career! The position
As Senior QA professional your main task will be to ensure patient safety, by delivering high-quality standards for our products. 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. Part of the job is to verify that studies are setup, conducted and documented with the right level of quality, for the diverse tasks from Manufacturing development such as: • establishing documentation for new products and processes
• ensuring compatibility of process aids and primary packaging
• stability and reference samples as well as specifications
As a team we are involved in complex cases with high attention, as well as innovation and digitalisation projects with stakeholders both locally and internationally. In these tasks, QA ensure and sets the quality direction as well as align across IFP QA organisation. Through strong communication and social skills, you will use your talents to set quality direction for stakeholders, both locally and internationally, and be a present character on the shopfloor. The role requires proactive oversight and the will to identify and ensure improvements for the area. You will get great opportunities for both personal and professional development, with growing responsibility depending on your skills and interests. Qualifications We are looking for someone that has the ability to set the right and balanced quality standards and ensure compliance within regulatory requirements. To succeed in this role, you:
• hold a Master’s degree in Biology, Engineering, Pharmacy, Chemistry or similar
• have GMP experience from a highly regulated industry
• have gained experience either in QA or production
• are fluent in English Knowledge of aseptic production and processes in a pharmaceutical environment will be an advantage. For this position we are open to evaluate more senior candidates that will be offered a QA Specialist role. As a person, you are a self-driven, proactive, and resourceful person. You thrive 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 30 people divided into three teams, and this position is in the Products & Processes team. The team 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
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594. Deadline
10 February 2023 We look forward to reading your application, and we will review applications received on an ongoing basis, so do not hesitate 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 why you are applying 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.
If so, you may be the person we are looking for to support our Quality Assurance (QA) unit for Injectable Finished Products Manufacturing Development (IFP ManDev). Read more below and apply now for a life-changing career! The position
As Senior QA professional your main task will be to ensure patient safety, by delivering high-quality standards for our products. 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. Part of the job is to verify that studies are setup, conducted and documented with the right level of quality, for the diverse tasks from Manufacturing development such as: • establishing documentation for new products and processes
• ensuring compatibility of process aids and primary packaging
• stability and reference samples as well as specifications
As a team we are involved in complex cases with high attention, as well as innovation and digitalisation projects with stakeholders both locally and internationally. In these tasks, QA ensure and sets the quality direction as well as align across IFP QA organisation. Through strong communication and social skills, you will use your talents to set quality direction for stakeholders, both locally and internationally, and be a present character on the shopfloor. The role requires proactive oversight and the will to identify and ensure improvements for the area. You will get great opportunities for both personal and professional development, with growing responsibility depending on your skills and interests. Qualifications We are looking for someone that has the ability to set the right and balanced quality standards and ensure compliance within regulatory requirements. To succeed in this role, you:
• hold a Master’s degree in Biology, Engineering, Pharmacy, Chemistry or similar
• have GMP experience from a highly regulated industry
• have gained experience either in QA or production
• are fluent in English Knowledge of aseptic production and processes in a pharmaceutical environment will be an advantage. For this position we are open to evaluate more senior candidates that will be offered a QA Specialist role. As a person, you are a self-driven, proactive, and resourceful person. You thrive 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 30 people divided into three teams, and this position is in the Products & Processes team. The team 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
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594. Deadline
10 February 2023 We look forward to reading your application, and we will review applications received on an ongoing basis, so do not hesitate 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 why you are applying 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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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 13.1.2023, 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.
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