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Project Manager*

St. Gallen


Our Business Unit Pharmaceutical Systems is one of the world's leading manufacturers of pharmaceutical primary packaging and analytical lab services.. More than 600 production lines in 13 countries worldwide produce more than 10 billion syringes, vials, ampoules, cartridges and special articles of tubing glass or polymer.

Project Manager*

Your Tasks
  • As Project Manager PMO you are our technology innovation driver.
  • You drive complex technology-innovation projects from idea along the project life cycle to industrialization by leading cross-functional project teams.
  • You secure the intellectual property of new technologies and align with the business unit on project contractual and financial conditions. You are responsible for project planning and -execution and ensure, that the project fulfils its scope and meets quality, delivery and cost targets. You ensure effective collaboration between project team members as well as internal and external stakeholders. You guide the project teams through the stage gate process and ensure successful milestone preparation. You identify project risks and present project status to upper management and steering committee.
  • You always ensure adherence to and monitoring of legal laws and internal regulations concerning IMSU / EHS / cGMP / Guidelines for pharmaceutical supplier industry / safety regulations for all involved parties.
Your Profile

In order to be successful in this role, you fulfill the following:

  • University degree in Life Science or Engineering (e.g. medical technology, pharmaceutical engineering, biotechnology, mechanical engineering, materials engineering etc.)

  • 4+ years of professional experience in project management and systematic problem solving within a GMP or Pharma-related environment

  • IPMA certification is a plus

  • Experience working with multidisciplinary and multi-cultural project teams

  • Experience with technology development of medical devices or pharmaceutical packaging

  • Knowledge of design control process and GMP (21 CFR 820; ISO 13485; ISO 15378)

  • Fluent in English (written and spoken) and in German (written and spoken)

  • Excellent communication and presentation skills

  • Strong analytical skills, structured working style and ability to prioritize

  • Strong interpersonal skills, ability to motivate and guide team members

Your Benefits