Process Engineer

Job description:

About us

Human health matters. That is why SCHOTT Pharma designs solutions grounded in science to ensure that medications are safe and easy to use for people around the world. Every day, a team of over 4,600 people from over 60 nations works at SCHOTT Pharma to contribute to global healthcare. The company is represented in all main pharmaceutical hubs with 16 manufacturing sites in Europe, North and South America, and Asia. SCHOTT Pharma AG & Co. KGaA is headquartered in Mainz, Germany and listed on the Frankfurt Stock Exchange as part of the SDAX. It is part of SCHOTT AG, which is owned by the Carl Zeiss Foundation.

Your Contribution

• You develop pioneer processes and introduce state-of-the-art technologies to manufacture innovative primary and secondary packaging products and secure their intellectual property
• You innovate while optimizing processing times, improving yield and reducing defects
• You are an expert in cleaning, coating, assembling, injection molding and/or packaging processes and technologies
• You execute complex innovation, customer specific and industrialization projects from the idea all the way to market launch
• You are responsible to plan technical work packages and deliver them according to quality, delivery and cost targets, in alignment with your project manager
• You know and understand production processes and their impact on the product functionalities and, vice versa, the impact of product designs on manufacturability and cost
• You have experience in a GMP regulated environment

Your Profile

• University degree in Life Science or Engineering (e.g. pharmaceutical engineering, biotechnology, mechanical engineering, process engineering, materials engineering etc.)
• 2+ years of working experience in process development of medical devices or pharmaceutical packaging
• Knowledge and experience with glass or polymer processes like cleaning, coating, assembling, injection molding and/or packaging processes
• Knowledge of equipment and process qualification and validation and related standards and regulations (21 CFR 820; ISO 13485; ISO 15378)
• Knowledge of statistical data analysis and Six Sigma certification
• Fluent in English (written and spoken) and in German (written and spoken)
• Structured working style and ability to plan and prioritize technical activities
• Creativity and ability to think out of the box and generate intellectual property
• Good interpersonal and communication skills with internal and external stakeholders

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

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, Elina Dominioni,

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

Profile description:

• University degree in Life Science or Engineering (e.g. pharmaceutical engineering, biotechnology, mechanical engineering, process engineering, materials engineering etc.)
• 2+ years of working experience in process development of medical devices or pharmaceutical packaging
• Knowledge and experience with glass or polymer processes like cleaning, coating, assembling, injection molding and/or packaging processes
• Knowledge of equipment and process qualification and validation and related standards and regulations (21 CFR 820; ISO 13485; ISO 15378)
• Knowledge of statistical data analysis and Six Sigma certification
• Fluent in English (written and spoken) and in German (written and spoken)
• Structured working style and ability to plan and prioritize technical activities
• Creativity and ability to think out of the box and generate intellectual property
• Good interpersonal and communication skills with internal and external stakeholders

We offer:

Flexible working hours

Canteen

Access to public transportation