Manufacturing GMP Scientist
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Kalundborg
Would you like to be part of the team that makes it happen? If so, we offer you a marvelous opportunity to widen your interest and skills in a position with great development opportunities, and fun challenges in an engaging working environment.
Apply now for a life-changing career!
The position
As a Manufacturing GMP scientist, when sudden challenges arise in our production, it will be your responsibility to ensure that action is taken so problems can be solved fast, efficiently and on the right quality level. In this way, we often get to be the people who gets everything up and running again – with the dedicated help of all the experienced operators, technicians, and other supporters.
Your key responsibilities will include:
Qualifications
To succeed in this role, you have:
As individual you are positive, corporative, action and solution orientated, and you work systematically, logically, and proactive. You can interact and communicate at all levels of the organisation, from operator to management, and you take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your key stakeholders. You take initiatives on your own, and to ensure commitment from your stakeholders, you have great focus on change management when introducing your ideas.
About the department
Our team is part of the Biotech & Rare Disease (BRD) Finished Products Kalundborg area that is part of our largest production complex in Novo Nordisk. Here we are app. 520 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We rely on our stabile/well-run/best-in-class packaging department and our newly established high-tech and high-volume filling facility. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include formulation, filling, freeze-drying, product inspection, assembly, and pack. We bring value to patients by delivering high-quality GMP compliant products in a timely and cost-efficient manner. We drive change by working actively with LEAN and always looking for improvements within our processes but also in the way we work together to make our products reach as many patients as possible.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
Contact
For further information, please contact Manager Ole Søgaard Iversen on phone +45 30 79 86 96.
Deadline
11 December 2022.
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.
Print job Send to e-mail
Apply now for a life-changing career!
The position
As a Manufacturing GMP scientist, when sudden challenges arise in our production, it will be your responsibility to ensure that action is taken so problems can be solved fast, efficiently and on the right quality level. In this way, we often get to be the people who gets everything up and running again – with the dedicated help of all the experienced operators, technicians, and other supporters.
Your key responsibilities will include:
- Coach, and assist your colleagues in GMP related tasks such as deviations and changes (delimitation, corrective & preventive actions, qualification etc.)
- Maintain high-level GMP overview on GMP and quality trends
- Setting direction and drive actions & projects across the department
- Drive preparation for and follow-up on authority inspections and internal audits
- Implement relevant systems related to GMP to improve our processes around GMP
Qualifications
To succeed in this role, you have:
- A MSc/BSc within pharmacy, chemical engineering, chemistry/biology or similar, preferably with 3-6 years of experience from the pharmaceutical or medical device industry or similar related areas
- Proven strong skills within GMP and coordination. You might have a long-term aspiration towards a leadership position.
- Thinking and active mindset with a broad and holistic perspective, seeing “The Big Picture” without losing sight or interest in important details
- A proficient level in English and Danish, or willing to learn Danish
As individual you are positive, corporative, action and solution orientated, and you work systematically, logically, and proactive. You can interact and communicate at all levels of the organisation, from operator to management, and you take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your key stakeholders. You take initiatives on your own, and to ensure commitment from your stakeholders, you have great focus on change management when introducing your ideas.
About the department
Our team is part of the Biotech & Rare Disease (BRD) Finished Products Kalundborg area that is part of our largest production complex in Novo Nordisk. Here we are app. 520 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We rely on our stabile/well-run/best-in-class packaging department and our newly established high-tech and high-volume filling facility. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include formulation, filling, freeze-drying, product inspection, assembly, and pack. We bring value to patients by delivering high-quality GMP compliant products in a timely and cost-efficient manner. We drive change by working actively with LEAN and always looking for improvements within our processes but also in the way we work together to make our products reach as many patients as possible.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
Contact
For further information, please contact Manager Ole Søgaard Iversen on phone +45 30 79 86 96.
Deadline
11 December 2022.
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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Kalundborg.
Jobbet er oprettet på vores service den 2.11.2022, 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
- Kalundborg
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