Technical Project Manager
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Gentofte
Are you passionate about project management and building relationships across the organisation? Are you a team player with strong stakeholder and project management skills, and do you have an eye for both strategic and operational details? Then you might be our new Senior Project Manager in our Project Management Office (PMO) in Gentofte. Apply now and contribute to the health of millions of people worldwide living with haemophilia and other rare disorders. The position Our manufacturing site faces an extensive and complex portfolio of projects initiated and executed over the coming years. Our production lines are facing several upgrades driven by e.g., introduction of new products; optimization initiatives; compliance or obsolescence of hardware and software. You will be key in driving projects throughout their entire lifecycle within our aseptic production portfolio roadmap that includes new technologies (equipment, machines, and processes), building facilities, IT and production line improvements. Thus, as a Senior Project Manager, you will be responsible for cross-functional projects that have a strategic impact to our aseptic manufacturing site. You will drive and facilitate projects with a GMP regulated environment and with a high level of complexity. You will engage with a wide range of internal and external stakeholders, and set the direction for your project team, whiles being responsible for all project metrics (cost, budget, time, etc).
Your main responsibilities will include: Planning, executing, and following up on all related tasks/processes related to scope, schedule, resources, cost, quality, and project risk. As a natural part of your projects, you will be in close dialogue with line of business and all levels of management at our production site, as well as external vendors. Ownership of cross functional project teams, project metrics (scope, time, plans, cost, etc.) Identify and manage key stakeholders and steering groups related to your projects. Actively contribute with learnings and experiences with rest of the PMO team to mature and strengthen our ability to run projects more efficiently. Qualifications To succeed in this role, you will have: A master’s degree related to Life Science, Engineering or similar. Minimum 3-5 years of experience as Project Manager, leading projects in e.g., operations, manufacturing development, quality assurance, preferably from a GMP regulated environment. Experience in working cross functionally and building relations with stakeholders and steering groups at different organizational levels. Certification within project management (e.g. MoP, PMP or PRINCE2) is an advantage Experience with aseptic production is an advantage. Excellent communication skills in both written and spoken English, preferably also in Danish. As a person, you have excellent communication skills. You are culturally savvy and able to build relations with stakeholders at all levels. You are a self-starter, that is capable to set direction and drive results independently. You possess leadership and interpersonal skills, and can engage people, build trust, and get commitment from stakeholders to support your projects and drive change. You are comfortable in a rapid changing and dynamic work environment and can prioritize and not lose sight of the bigger picture. About the department You will be part of a dynamic and ambitious Project Management Office in the Operational Excellence department, where our Project Managers execute small to large projects across our production site. The department Operational Excellence consists of a Project Management Office, Digitalisation and MI and Process Excellence teams. We support the Aseptic Production which is a part of the BRD Finished Products Gentofte and Vaarloese production site situated close to Copenhagen. Here we are app. 725 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We are producing at full speed on existing lines while building and ramping up new state of the art facilities. 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 in 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 are also stiving 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 Associate Manager Serap Sahin +45 3075 8936. Deadline 18 February 2024. We will review applications and conduct interviews on an ongoing basis, so we encourage you to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. In addition, please avoid the use of photos in your CV. This provides a better and more fair process. 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.
Your main responsibilities will include:
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 29.1.2024, 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.
- Projektleder
- Gentofte
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