Quality Assurance Professional for QC
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Bagsværd
Do you want to be a part of quality assurance (QA) for Manufacturing Development and Quality Control (QC)? Are you eager to set direction and to ensure compliance, in close work with your stakeholders? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle? Then keep reading. The position
In this position you will contribute to ensure a high level of quality and set the quality direction for QC processes and activities performed in Injectable Finished Products.
Typical tasks will be:
• Reviewing and approving documentation e.g., Deviations, Laboratory Investigations, Change Requests, SOPs. Furthermore, approval of equipment qualification and approval of validation of analytical or microbial methods could be an area of responsibility.
• QA presence: being physically present in QC laboratories a few days a month.
• Advising stakeholders to keep the right level of quality.
• Participating and presenting cases when we are inspected from authorities from around the world.
• Improving processes in own QA area.
Participation in projects within core competencies is also an opportunity. Qualifications
To succeed in this role, you:
• hold a university Bachelor or Master in Pharmacy, Engineering, Biology, Chemistry or similar.
• have experience in a pharmaceutical company, ideally also within QC and/or in a QA role.
• are proficient in English.
If you have been working within validation of analytical methods, equipment qualification or microbial analysis, it will be seen as an advantage. About the department
The department is QA for Injectable Finished Product Manufacturing Development (IFP ManDev). ManDev is the link between R&D and manufacturing sites and drive upscaling, improvements, product and process support, and development of new chemical and microbial analytical methods. Furthermore, the responsibility for the Danish QC laboratories in Bagsværd and Hillerød along with support to other global QC laboratories lies within ManDev’s responsibility.
You will be a part of the QA team which covers Analytical and Microbial Competence Centres and QC laboratories located in Bagsværd and Hillerød.
The team consist of 12 QA colleagues who take pride in their work and value a good working environment. We are situated in Bagsværd, Denmark.
The department consist of ca. 40 employees and support various functions in IFP Man Dev. Contact
For further information, please contact Manager Christoffer Bjarrum Winther +45-30752285. Deadline
Deadline to apply for this position is February 11th, 2024.
Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline.
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.
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.
In this position you will contribute to ensure a high level of quality and set the quality direction for QC processes and activities performed in Injectable Finished Products.
Typical tasks will be:
• Reviewing and approving documentation e.g., Deviations, Laboratory Investigations, Change Requests, SOPs. Furthermore, approval of equipment qualification and approval of validation of analytical or microbial methods could be an area of responsibility.
• QA presence: being physically present in QC laboratories a few days a month.
• Advising stakeholders to keep the right level of quality.
• Participating and presenting cases when we are inspected from authorities from around the world.
• Improving processes in own QA area.
Participation in projects within core competencies is also an opportunity. Qualifications
To succeed in this role, you:
• hold a university Bachelor or Master in Pharmacy, Engineering, Biology, Chemistry or similar.
• have experience in a pharmaceutical company, ideally also within QC and/or in a QA role.
• are proficient in English.
If you have been working within validation of analytical methods, equipment qualification or microbial analysis, it will be seen as an advantage. About the department
The department is QA for Injectable Finished Product Manufacturing Development (IFP ManDev). ManDev is the link between R&D and manufacturing sites and drive upscaling, improvements, product and process support, and development of new chemical and microbial analytical methods. Furthermore, the responsibility for the Danish QC laboratories in Bagsværd and Hillerød along with support to other global QC laboratories lies within ManDev’s responsibility.
You will be a part of the QA team which covers Analytical and Microbial Competence Centres and QC laboratories located in Bagsværd and Hillerød.
The team consist of 12 QA colleagues who take pride in their work and value a good working environment. We are situated in Bagsværd, Denmark.
The department consist of ca. 40 employees and support various functions in IFP Man Dev. Contact
For further information, please contact Manager Christoffer Bjarrum Winther +45-30752285. Deadline
Deadline to apply for this position is February 11th, 2024.
Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline.
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.
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 22.1.2024, 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
- Bagsværd
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