Senior QA Professional for small molecules
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Måløv
Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of products for clinical trial s and be part of an exciting growth journey within our small molecules portfolio? If so, we have an exciting possibility waiting for you as QP delegate in Contract Manufacturing Organisations (CMC) Oral Product (OP) Development QA. The position is based in Måløv, Denmark.
The position
As senior QA Professional, you will be responsible for delivering best-in-class quality assurance of our new manufacturing processes and drug product for clinical trials. In your daily work you will challenge and approve documents in connection with development, manufacture, stability, and status assignment of clinical batches.
Novo Nordisk is expanding within small molecules and in this position, you will be part of building up our QMS and will primarily work with release from Contract Manufacturing Organisations (CMO). It will be possible to work with both API and DP release. In addition, you will be a part of our development projects ensuring our products used in clinical trials are following the information provided to Health Authorities worldwide. Office presence expected at minimum three days weekly.
Qualifications You hold a MSc in Pharmacy, Engineering, Biology, Chemistry or similar. Your education should as a minimum support the demands and expectations to a “Qualified Person” from the Danish Medicines Agency (Lægemiddelstyrelsen). 7+ years of experience with GMP and quality assurance and has experience with batch release/status assignment. The ideal candidate has been working as a QP delegate for several years and has worked with small molecules and API/solid dosage forms (tablets) in a GMP environment. Further, CMO experience will be and advantage.
The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems.
You have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.
You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. You thrive in a dynamic environment, where teamwork is on top of the agenda, and you like working with many different stakeholders – internally and externally.
We operate in an international company and the position therefore requires proficiency in English and Danish.
About the department
You will become part of a department (CMC OP Dev QA & Analysis QA) consisting of two teams where we currently are 25 dedicated colleagues. We are currently building up competencies within small molecules and therefore you will be reporting directly to the QA Director. You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
Working at Novo Nordisk
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.
We offer a modern working environment; free flow of coffee and tea, fruit, canteens serving world cuisine which includes both meat- and vegetarian options, take-out dinner options, access to internal fitness centers at our sites, bike repair at work, electric car charge stations, health insurance, social clubs, team outings and so much more.
Contact
For further information, please contact QA Director Casper Yding +45 3079 7015
Deadline
October 1st, 2023
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.
The position
As senior QA Professional, you will be responsible for delivering best-in-class quality assurance of our new manufacturing processes and drug product for clinical trials. In your daily work you will challenge and approve documents in connection with development, manufacture, stability, and status assignment of clinical batches.
Novo Nordisk is expanding within small molecules and in this position, you will be part of building up our QMS and will primarily work with release from Contract Manufacturing Organisations (CMO). It will be possible to work with both API and DP release. In addition, you will be a part of our development projects ensuring our products used in clinical trials are following the information provided to Health Authorities worldwide. Office presence expected at minimum three days weekly.
Qualifications
The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems.
You have a profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production and hence can navigate without adding complexity.
You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks. You thrive in a dynamic environment, where teamwork is on top of the agenda, and you like working with many different stakeholders – internally and externally.
We operate in an international company and the position therefore requires proficiency in English and Danish.
About the department
You will become part of a department (CMC OP Dev QA & Analysis QA) consisting of two teams where we currently are 25 dedicated colleagues. We are currently building up competencies within small molecules and therefore you will be reporting directly to the QA Director. You will be part of a strong culture, where we strive for high psychological safety, give regular feedback, and understand that the most important thing we have is our people. Our main purpose is to safeguard patient safety and ensure product quality and compliance in the CMC area, and ultimately release drug candidates for clinical trials. As part of Novo Nordisk Quality, we support the business and strive for simplicity every single day, to ensure Novo Nordisk’s critical delivery of medicine to patients.
Working at Novo Nordisk
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.
We offer a modern working environment; free flow of coffee and tea, fruit, canteens serving world cuisine which includes both meat- and vegetarian options, take-out dinner options, access to internal fitness centers at our sites, bike repair at work, electric car charge stations, health insurance, social clubs, team outings and so much more.
Contact
For further information, please contact QA Director Casper Yding +45 3079 7015
Deadline
October 1st, 2023
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.
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 5.9.2023, 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
- Måløv
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