Global Manufacturing Science and Technology API Project Manager

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Global Manufacturing Science and Technology API Project Manager
Manufacturing Science & Technology

Are you an experienced project manager with a data-driven mindset? And are you looking to help shape the future of a rapidly developing pharmaceutical company with global operations?

The GMS&T API team is a global team, located in Copenhagen, with a focus to bring our API production sites closer together and ensure implementation of best practice processes and procedures.

In this position, you will be an integral part of Xellia Pharmaceuticals’ Global Manufacturing Science and Technology (GMS&T) API team, where you will perform project management of tech transfers and standardization activities, typically with a high degree of cross-functional involvement. In addition to managing projects, you will serve as general representative for API process performance.

You will coordinate activities with our many partners in e.g. R&D, Production, Regulatory Affairs, Quality and Engineering, involving all aspects of project management, from initial scoping to implementation and benefit realization.

Your key tasks include:

  • Manage all project aspects to ensure a robust commercial scale-up and timely implementation of new API products or processes
  • Develop and maintain standards for implementation of R&D tech transfer projects across all API sites
  • Ensure that other PM’s act accordingly when relevant across sites
  • Support R&D scientists with production scale experience during development phase
  • Propose and support API technological improvement initiatives (e.g. continuous improvements, CI) in the commercial phase of the product lifecycle
  • Partner with other GMS&T teams to develop, review and implement Xellia’s global standards, guidelines and SOPs ensuring best practice across Xellia API sites
  • Manage standardization of best practice across sites
  • Ensure knowledge sharing of process improvements and product/process issues across all Xellia API production sites
  • Serve as scientific and technical representative for API process-related issues at Xellia API sites as well as third party API manufacturing sites
  • Partner with site MS&T and other relevant stakeholders to routinely evaluate process performance to ensure all Xellia API products are sufficiently monitored and maintain satisfactory process capabilities
  • Support local MS&T to resolve complex reduction in capability or performance
  • Ensure knowledge sharing of process improvements and product/process issues across all Xellia API production sites

Join a global function and grow
As you step into a global organization, you collaborate closely with your colleagues in other departments and at Xellia´s other manufacturing and business locations, which will possibly involve some traveling.

You will be expected to deliver tangible results with high impact by managing cross-functional and international projects and be given an opportunity to grow, working in an international well-funded company with a focused growth strategy.

A skilled coordinator with a personal drive for results
To succeed in this position, you have a superior overview with an analytical and data-driven mindset. You handle issues pro-actively, and you are known for your ability to communicate with numerous and versatile stakeholders with a positive attitude.
Moreover, you have:

  • Bachelor's degree in engineering (chemical, industrial, pharmaceutical, mechanical), pharmaceutical sciences, chemistry or any related science degree required.
  • Master of Science degree preferred.
  • 5+ years of professional experience in the pharmaceutical industry is preferred
  • Strong experience with project management and technical transfers
  • Strong knowledge of pharmaceutical unit operation and quality requirements in the pharmaceutical industry, including regulatory and GMP requirements
  • Strong analytical skills, with ability to process complex data sets into useful information
  • English at business level required, Danish preferred

Deadline and additional information
Please submit your CV and cover letter as soon as possible and no later than 12 February – we will begin interviewing at an ongoing basis and the position will be filled when we have the right candidate. If you have any questions regarding the position, please contact Senior Manager Global Manufacturing Science and Technology API CPH, Rune Prior on phone +45 21 91 67 66

Xellia Pharmaceuticals is owned by Novo Holding A/S and is a specialty pharmaceutical company leading in the development, manufacture and supply of anti-infective treatments. Headquartered in Copenhagen, Denmark, Xellia has global facilities in Europe, North America, and Asia, currently employing over 1700 people. With over 100 years of industry experience in developing last resort treatments for infectious diseases, Xellia is focused on the supply of products which not only save lives, but also improve and enhance patients’ quality of life. Together with us, you can help lead the fight against bacterial infections.
Read more about Xellia Pharmaceuticals here


Information og data

Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 14.1.2021, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Projektleder
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