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Description

About us

Gesundheit ist entscheidend. Deshalb entwickelt SCHOTT Pharma wissenschaftlich fundierte Lösungen, die gewährleisten, dass Medikamente für Menschen auf der ganzen Welt sicher und einfach zu verwenden sind. Über 4.600 Menschen aus über 60 Nationen arbeiten bei SCHOTT Pharma jeden Tag daran, einen Beitrag zur weltweiten Gesundheitsversorgung zu leisten. Mit 14 hochmodernen Werken in Europa, Nord- und Südamerika sowie Asien ist das Unternehmen in allen wichtigen Pharma-Märkten vertreten. Die SCHOTT Pharma AG & Co. KGaA hat ihren Hauptsitz in Mainz und ist im MDAX an der Frankfurter Wertpapierbörse gelistet. Sie ist Teil der SCHOTT AG, einem Unternehmen der Carl-Zeiss-Stiftung. In diesem Sinne setzt sich SCHOTT Pharma nachhaltig für Gesellschaft und Umwelt ein und hat sich verpflichtet bis 2030 klimaneutral zu werden.

Your Contribution
  • You drive complex innovation and customer specific projects from idea all the way to market launch by leading cross-functional project teams.

  • You are responsible for project planning, execution and ensure that the project fulfils its scope and meets quality, delivery and cost targets.

  • You guide the project teams through our stage gate process and ensure successful milestone preparation.

  • You identify project risks or issues and present possible countermeasures to the steering committee to drive decisions.

  • You secure the intellectual property of new products and technologies and align with the business unit on project contractual and financial conditions.

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

  • 4+ years of project management experience with experience with product/process development of medical devices or pharmaceutical packaging

  • Experience working with multidisciplinary project teams in complex organizations and ability to motivate and guide team members

  • Knowledge of design control process, process validation and related standards (21 CFR 820; ISO 13485; ISO 15378)

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

  • Excellent communication and presentation skills

  • Capability to master the big picture but also technical details when required

  • Strategic mindset and business acumen with a structured working style and ability to prioritize

Your Benefits

SCHOTT's openness to promote your further development is just as great as our additional benefits. Ranging from active health management via flexible working hours and hybrid work all the way to corporate pension plans: everything geared to suit your goals and needs. Discover a special corporate culture where everyone has the opportunity to develop their entire potential.

At SCHOTT, you can expect a unique corporate culture where we emphasize equity, diversity, and inclusion. We know: motivated and committed employees are the precondition for the success of our company.

Flexible working hours; Access to public transportation; Canteen; Holistic corporate health management; Team Events; paid vacation days, holidays and sick time

Please feel free to contact us

You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future. Do you want to be successful with us? Then, please send us your application: SCHOTT Pharma Schweiz AG, Human Resources, Kristina Ettemeyer, +41712740849

*At SCHOTT, it's your personality that counts - not your gender, your identity, or origin.



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

  • 4+ years of project management experience with experience with product/process development of medical devices or pharmaceutical packaging

  • Experience working with multidisciplinary project teams in complex organizations and ability to motivate and guide team members

  • Knowledge of design control process, process validation and related standards (21 CFR 820; ISO 13485; ISO 15378)

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

  • Excellent communication and presentation skills

  • Capability to master the big picture but also technical details when required

  • Strategic mindset and business acumen with a structured working style and ability to prioritize


Holistic corporate health management

Flexible working hours

Team Events

Canteen

Access to public transportation