Senior Project Manager with HVAC experience
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Gentofte
Do you have experience in implementing HVAC systems in Pharmaceutical Production and do you have strong project manager skills? Are you looking for an exciting opportunity to drive the HVAC process across Novo Nordisk through global collaboration? Then join us and utilize your knowledge and skills in an exciting organization, where you will get challenged, grow, and expand your capabilities to the fullest. Apply now for a life-changing career.
The position
As Senior Project Manager for our HVAC Process across Novo Nordisk you are expected to:
The main drivers for the projects you lead are to simplify, standardise and keep our processes in compliance – and bring the Process into the future by digitalization. By excellent project execution, you will successfully deliver solutions to key challenges across Product Supply.
You will be part of a great team covering all aspects of the production processes, including the requirements to establish, operate, and maintain facilities and environment used for manufacturing. We have a strong focus on making a difference in close collaboration with the production sites by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations. We also concentrate on innovation and optimization of the processes in our production facilities in Biotech and Rare Disease (BRD) area and utilise our test laboratory to further increase focus on science and implementation of new technology.
Qualifications
To succeed in this role, you have:
As a person you are inspiring and motivating, a strong innovator, that shrives for continuous improvement, and you have a drive to set and reach ambitious targets on new ground. As you have a structured approach to your work, you can juggle several tasks while prioritising your efforts optimally by keeping the bigger picture in mind. Whilst you can expect a high degree of independence in this position, you also act as a team player with great ability to build strong working relations, take charge of a group and collaborate with people across boundaries.
We expect you to be a good communicator, including the ability to target your communication in alignment with other areas to a broad set of stakeholders at all organisational levels ensuring clear argumentation to ease decision making for senior management.
About the department
Our team is a part of BRD Manufacturing Development & Quality Control and has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible.
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. 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
If you have any questions about the position or just want to get a feeling of the department and our exciting road ahead, please do not hesitate to call Associate Manager Ditte Kivsmose Kaldor at +45 30 75 77 67.
Deadline
1 January 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.
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The position
As Senior Project Manager for our HVAC Process across Novo Nordisk you are expected to:
- Facilitate the process group network across NN Product Supply areas and within your own SVP area. The process group consists of members from all our production sites, QA, and subject matter experts.
- Have knowledge about authority requirements and industry practice to HVAC systems, including FMS/BMS. It will be an advance if you are engaged in an extern HVAC forum.
- Support Production sites about HVAC.
- Manage the project portfolio within the HVAC process.
- Drive compliance improvements, continuous improvements, digitalisation projects in the process.
- Work independently with global projects varying from small Quality Management Systems (QMS) projects to large investment. projects.
The main drivers for the projects you lead are to simplify, standardise and keep our processes in compliance – and bring the Process into the future by digitalization. By excellent project execution, you will successfully deliver solutions to key challenges across Product Supply.
You will be part of a great team covering all aspects of the production processes, including the requirements to establish, operate, and maintain facilities and environment used for manufacturing. We have a strong focus on making a difference in close collaboration with the production sites by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations. We also concentrate on innovation and optimization of the processes in our production facilities in Biotech and Rare Disease (BRD) area and utilise our test laboratory to further increase focus on science and implementation of new technology.
Qualifications
To succeed in this role, you have:
- A Master’s Degree or Ph.D. in Engineering, Chemistry, Pharmacy, Biology, Project Management or similar.
- Experience with driving projects across the organisation.
- Relevant business experience such as cLEAN, Six Sigma, communication and presentation skills for top management or cross organisational network.
- Experience with HVAC systems and GMP in Pharmaceutical Production.
- Full professional proficiency in English and some experience with Danish.
As a person you are inspiring and motivating, a strong innovator, that shrives for continuous improvement, and you have a drive to set and reach ambitious targets on new ground. As you have a structured approach to your work, you can juggle several tasks while prioritising your efforts optimally by keeping the bigger picture in mind. Whilst you can expect a high degree of independence in this position, you also act as a team player with great ability to build strong working relations, take charge of a group and collaborate with people across boundaries.
We expect you to be a good communicator, including the ability to target your communication in alignment with other areas to a broad set of stakeholders at all organisational levels ensuring clear argumentation to ease decision making for senior management.
About the department
Our team is a part of BRD Manufacturing Development & Quality Control and has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible.
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. 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
If you have any questions about the position or just want to get a feeling of the department and our exciting road ahead, please do not hesitate to call Associate Manager Ditte Kivsmose Kaldor at +45 30 75 77 67.
Deadline
1 January 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.
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 Gentofte.
Jobbet er oprettet på vores service den 12.12.2022, 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.
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