Senior Project Manager, Manufacturing Development

Job title:

Senior Project Manager, Manufacturing Development

Company:

Novo Nordisk

Job description

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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Senior Project Manager, Manufacturing DevelopmentCategory: ManufacturingLocation:Bagsværd, Capital Region of Denmark, DKDo you want to work with improvement projects for Intermediates and critical Raw Materials processes to continually support and strengthen Novo Nordisk as a world-leading insulin and GLP-1 manufacturer? If so, we offer you the opportunity to be part of the Project Office in Manufacturing Development in PS API (Active Pharmaceutical Ingredients). In our team, high engagement, innovation and ambition are key in executing projects, set to improve capacity, compliance, and quality of our Drug Substances manufacturing processes.Apply now for a life-changing opportunity!The positionYou will be heading up project groups with members from e.g., Manufacturing Development, Global Contract Manufacturing, QA, Regulatory Affairs, QC and Sourcing. Your role will be to inspire and motivate the project group to deliver excellent results by ensuring clear project scopes, use of risk management and project plans that secure transparency for all key stakeholders. You will be responsible for related communication to stakeholders (including Management).You will be working close with our Scientists in Manufacturing Development, our colleagues in Global Contract Manufacturing and Strategic Sourcing to choose and execute projects aligned with the PS API Strategy. You will have a key role in ensuring coordination between PS API Manufacturing Development and various departments in the Sourcing & Supply organisation. You can also look forward to:

• driving a portfolio of cross-organisational projects, which includes driving and supporting development projects related to CMO’s on intermediates for GLP and Insulin Drug Substances
• identifying improvement ideas, in collaboration with stakeholders, to ensure a continuous improvement of the processes

You will also be involved in regulatory activities. Thus, it is important, that you have an interest in the documentation needed for the health authorities in collaboration with Regulatory Affairs and other stakeholders.Qualifications
To succeed in this role, we imagine that you have:

• an academic Degree (B.Sc., M.Sc., Ph.D. or similar) in pharmacy, engineering, biotechnology, or other Life Sciences
• some years of experience in medical production or development
• experience with project management or project coordination
• ability to work in cross-functional teams as well as with external stakeholders
• interest in exploring the scientific part of the projects to be able to support the project members and guide the management
• full professional proficiency in written and spoken English

On a personal level, you are motivated, pro-active, and self-driven and have a structured approach to your work, with high interest and passion for achieving results. You have a global mindset and enjoy building relations across the organisation with multiple stakeholders, work cultures and geographies.About the department
In PS API Manufacturing Project Office, Life Cycle Management we are a team of Project Managers and Senior Project Managers focusing on insulin and GLP-1 Drugs Substances for marketed products. We execute projects for process optimisation set to improve capacity and quality and reduce cost and we support project governance that secures continuous optimisation across PS API.In the team we are proud of our balance between ambitious goals, working hard and maintaining a healthy and fun approach to our tasks. You will be joining a skilful and inclusive team, where collaboration and personal development are in focus.Working at Novo NordiskAt Novo Nordisk, we don’t wait for 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 manufacturing, to marketing and sales – we’re all working to move the needle on patient care.Contact
For further information, please call Portfolio Vice President, Ulla Falkenberg on +45 3075 8890.Deadline16 June 2024.Applicants will be reviewed and called in for interviews on an ongoing basis, so please apply as soon as you can. 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 to 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.

Expected salary

Location

Bagsværd, Hovedstaden

Job date

Sun, 09 Jun 2024 03:30:09 GMT

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