Quality Professional with QP delegate responsibility for tablet product
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Måløv
- Quality
- Måløv
Do you want to be part of the team bringing Rybelsus to patients all over the world?
Novo Nordisk has built a new factory in Måløv which will be part of setting new standards for diabetes treatment. To succeed with this ambition, we need people with high level of team spirit, having high engagement and who thrives in a constant changing environment.
About the department
In 2004 an ambitious and path-breaking journey began for us to become the first medical company delivering GLP-1-based tablets to the market. This year we delivered Rybelsus tablets to the first patients and going forward millions of patients with type-2 diabetes will have an oral alternative to injectable preparation. This is a result of competent, innovative and engaged employees’ efforts across the organization, who are proud to use their dedication to make totally new standards within the diabetes treatment. Join us at our journey – a possibility to make a personal and professional development.
Oral Finished Products QA is a department which employ approximately 30 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, Manufacturing development and the quality management system as well the release of tablets for the market.
In OFP QA we make a huge effort for you as a new employee to be off to a good start. During the first few days you will spend time with other new employees in the OFP area, where you will get an exciting introduction to OFP. The manager will welcome you, and a colleague will act as a mentor and go through your individual training plan. We know how important it is, and we are looking forward to meeting you.
The job
You will act as QP delegate, and you will have the overview of the processes within production of oral medicinal products. Your focus will be assuring that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements.
In close cooperation with your colleagues in QA, you act as a QA for the Oral Finished Product area. You contribute to finding solutions for ad hoc questions and challenges within cGMP compliance. You will review and approve quality documentation from our stakeholders including deviations, change requests, SOPs, manufacturing batch records and other relevant documents as well as executing the QP release and perform batch confirmation.
Our continuing high level of audit and inspection readiness is on top on your agenda.
This means that you work with QA oversight where you proactive, together with your colleagues, will identify areas where our compliance can be strengthened.
You have a risk based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
Qualifications
You hold an academic degree as pharmacist and have at least 2 years of experience from a pharmaceutical or medical device organisation, where you have gained a solid and up-to-date knowledge of quality and GMP requirements. You must be fluent in both written and English and preferrably also danish.
The ideal candidate has thorough knowledge within manufacturing and/or quality assurance of oral solid dosage forms.
You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we simplify and improve our processes. You focus on results and quality – and contribute to the right level of compliance.
Contact
For further information, please contact Sine Godiksen +45 3075 1426.
We will conduct interviews continually.
Deadline
Deadline to apply for this position is november 16th 2020
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 12.11.2020, 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
- Måløv
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