Operation Responsible for Downstream Processing
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Hillerød
Are you motivated by working in a dynamic and international project environment with a team of inspiring and enthusiastic colleagues that turn ideas into solutions? Are you thrilled by the idea of being involved in the establishment of a large, new capacity expansion facility and shaping future technologies for API production at Novo Nordisk? Those are just some of the opportunities you’ll have when you join our fantastic team. We have several open positions for Operation Responsible profiles with different levels of experience in our new facility project. The position As an Operation Responsible you will drive the project execution within your area of responsibility, be involved in collaborative design development with suppliers and with oversight to ensure the solution is built according to the design. Alongside the team, you will be at the core of ensuring the best possible design, delivering a solution we can be proud of in 20 years! Your key tasks will include: Participation in project execution and establishment of the new facility and downstream production processes. Review of supplier design documentation. Align on the technical decisions together with our local project team Review of Factory Acceptance Test (FAT), Site Acceptance Test (SAT) protocols and reports, oversight during verification tests. Responsible for the API purification process within your area Establishing the working procedures (SOPs) for the process and equipment, including development of the associated training of users. You will work in collaboration our dynamic and social project team consisting of 10 colleagues with various background, nationality and seniority, the Work Package Owner (WPO), local specialist, IT/Automation specialist as well as engineering partners during the project phase. Some travel activities must be expected.
Qualifications To succeed in this role, you have: An academic degree within engineering, pharmaceutical science or similar +3 years of within life-science industry and working with cGMP Experience within API production / validation will be highly advantageous. Experience with working in, and coordinating across, a multi-disciplinary team Full professional proficiency in English. We expect you to be able to work independently and you think it’s fun to drive and work with several activities at the same time. You have a forward-looking mindset and work in a structured manner to reach our common goals. Further, you enjoy learning and sharing knowledge and information with others. You’re able to collaborate and coordinate across several disciplines in an international, multicultural and dynamic environment. About the department Join us at 25L API (Active Pharmaceutical Ingredient) Capacity Expansion and become a part of one of Novo Nordisk’s most significant expansion projects, embedded in Biotech & Rare Disease (BRD). In BRD, we are building a new API production facility in Hillerød that will employ around 340 colleagues. The highly automated production facility will be equipped with state-of-the-art technology that is flexible to accommodate new processes and products. It will also expand our portfolio of clinical late phase products and increase our capacity to serve more people living with rare disease and serious chronic diseases. To drive the project and reach the initial phase of production, we need your support. We do not only drive change for our patients – we also drive life-changing careers for our employees by promoting a learning culture with high levels of trust, innovation and development throughout the organization. Are you ready to join the project team and our journey?
Working at BRD, Novo Nordisk Biotech & Rare Disease (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. 3000 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.
Contact
If you would like to discuss further, you are welcome to contact Manager Helle Baltzer Hattel at (+45 3079 7266) or Senior Project Engineering Manager (Downstream WPO) Kim Vincentz Andersen at +45 34 48 69 79 Deadline
29 October 2023. Applications will be screened on an ongoing basis, so you are encouraged 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.
Qualifications To succeed in this role, you have:
Working at BRD, Novo Nordisk Biotech & Rare Disease (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. 3000 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.
Contact
If you would like to discuss further, you are welcome to contact Manager Helle Baltzer Hattel at (+45 3079 7266) or Senior Project Engineering Manager (Downstream WPO) Kim Vincentz Andersen at +45 34 48 69 79 Deadline
29 October 2023. Applications will be screened on an ongoing basis, so you are encouraged 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 28.9.2023, 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.
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