Engineering Manager
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Kalundborg
Would you like to join a dynamic global company and work on an exciting new project? Are you interested in the opportunity to establish potential new API manufacturing facilities that bridge new and automated technologies with strong know-how and expertise in biotech manufacturing? This could be your chance to influence the technical direction of the project and make sure it follows design standards. Apply now for a life-changing career as an Engineering Manager! The position
In this role you can look forward to managing the scope of the project activities in terms of investigating design, constructability, schedule, and cost for a potential new production facility. The key design principle will be to implement the best-in-class standards from other production facilities. You will be the main person responsible for overseeing that our Project Execution Model is used in the best possible way in the project. Your focus will be on implementing known solutions as well as developing new design solutions where relevant. You will take an active part in integrating with engineering partners and collaborating with contractors while supervising their activities. You will also proactively manage project risks and develop standards to ensure structure and transparency. Your tasks and responsibilities will include: Facilitating the design and technology discussions across teams Supporting colleagues in solving complex challenges Facilitating and guiding the design, building and optimisation of systems and equipment for the production Developing standards and guidelines The focus of your role will be on providing innovative, efficient, and effective solutions; as well as on the consistency of work, cross-disciplinary quality, reviews and compliance with pharmaceutical codes and regulations. Qualifications We imagine that a successful candidate will have: 5+ years of relevant engineering management experience, preferably within medical production, such as Active Pharmaceutical Ingredient (API) production or finished products A master's or bachelor's degree in biomanufacturing engineering, mechanical engineering or similar, although the right experience will be more important than a degree Solid understanding of process equipment, automation and working in a Good Manufacturing Practice (GMP) regulated environment Profound insight into systematic problem-solving Excellent communication skills in both written and spoken English with the ability to create clear and high-quality presentation materials. On a personal level, you are a self-starter who thrives in driving tasks independently. You have excellent analytical, planning and organizing skills, which enables you to continuously set direction, keep an overview of the state of progress and prioritize accordingly. With your strong logical ability, you succeed in transforming complex information from the scoping phase to execution and completion. At Novo Nordisk, we will appreciate your curiosity and eagerness to challenge status quo in a respectful way to ensure that pragmatic solutions are brought forward in a swift manner. This will require an independent approach combined with an agile mindset and good stakeholder management skills. It will be helpful if you can network, build trust in your relationships and get commitment from internal and external stakeholders. About the department Today, 3,200 employees of Novo Nordisk Kalundborg produce half of the world’s insulin and a number of biopharmaceutical products. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. By joining Novo Nordisk Manufacturing in Kalundborg, we promise you a developing career, where you will be met with trust and responsibility by dedicated colleagues with diverse backgrounds in a successful company with a higher purpose and an inclusive environment. Together, we make a difference every day for more than 30 million people living with diabetes and other chronic diseases. This is your opportunity to be part of our exciting journey. Read more at: novonordisk.com/kalundborg-careers Working at Novo Nordisk At Novo Nordisk, we don’t wait for a change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Engineering Manager, Rasmus Schou Johansen +45 3079 0558. Deadline 27 March 2023. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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.
In this role you can look forward to managing the scope of the project activities in terms of investigating design, constructability, schedule, and cost for a potential new production facility. The key design principle will be to implement the best-in-class standards from other production facilities. You will be the main person responsible for overseeing that our Project Execution Model is used in the best possible way in the project. Your focus will be on implementing known solutions as well as developing new design solutions where relevant. You will take an active part in integrating with engineering partners and collaborating with contractors while supervising their activities. You will also proactively manage project risks and develop standards to ensure structure and transparency. Your tasks and responsibilities will include:
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 10.3.2023, 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
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 7. november 2024 | 57 |
| 6. november 2024 | 57 |
| 5. november 2024 | 57 |
| 4. november 2024 | 50 |
| 3. november 2024 | 52 |
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| 10. oktober 2024 | 41 |
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| 8. oktober 2024 | 38 |