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.

• As Team Leader you lead, develop and motivate a team of experienced product engineers (up to 6 FTEs).

• You develop the expertise of your team in alignment with the Competence Fields strategy and make sure that the technical knowledge is well organized and shared within Glass Syringes and outside.

• You assign your team members to innovation and customer specific projects and support them to plan and execute their work packages.

• You guide the project team members to develop high quality products by following the design control process and preparing robust design reviews.

• You identify technical risks or issues and support the team to define possible countermeasures or drive decisions.

• You secure the intellectual property of new products and ideas.

• You analyze project requests for their technical feasibility and prepare estimates of costs and timeline of product development work packages.

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

• 3+ years of project management experience and min. 2 years of team leadership experience

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

• Experience with product/process development of medical devices or pharmaceutical packaging

• 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)

• Capability to master the big picture and technical details when required

• Strategic mindset and business acumen with excellent communication and presentation skills

• Structured working style and ability to prioritize

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

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, Marjon Kundert, +41712740883

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

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

• 3+ years of project management experience and min. 2 years of team leadership experience

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

• Experience with product/process development of medical devices or pharmaceutical packaging

• 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)

• Capability to master the big picture and t