Quality Expert R&D and Global Engineering
vor 3 Wochen
SCHOTT is a leading international technology group in the areas of specialty glass and glass-ceramics. With more than 130 years of outstanding development, materials and technology expertise we offer a broad portfolio of high-quality products and intelligent solutions. SCHOTT is an innovative enabler for many industries, including the home appliance, pharmaceutical, electronics, optics, life sciences, automotive and aviation industries. SCHOTT strives to play an important part of everyone's life and is committed to innovation and sustainable success. The parent company, SCHOTT AG, has its headquarters in Mainz (Germany) and is solely owned by the Carl Zeiss Foundation. As a foundation company, SCHOTT assumes special responsibility for its employees, society and the environment.
About usOur 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.
Your ContributionYou are result-driven and combine the dynamics of a development environment with the diligence required for QM processes.
You maintain and develop the R&D QMS and ensure compliance.
You manage the R&D CAPA process and perform internal audits acc. to ISO 15378 and ISO 13485.
You drive continuous improvement within R&D and on its interfaces.
You ensure compliant harmonized development documentation.
You enable your colleagues to be easily compliant to our QMS by guidance and training.
You hold a University degree in Engineering, Life Science or similar.
You have 3+ years of working experience in pharmaceutical packaging-, medical device-, or pharma industry with development environment and contact to QMS acc. to ISO 15378 or ISO 13485 or similar.
Diligence, proactive and structured independent working belong to your strengths.
You have knowledge in QMS and document management, as well as GDocP.
Strong presentation and moderation skills and a drive to accuracy describe your personality.
You took part in or lead audits, or at best are a certified auditor, preferably ISO 13485 / ISO 15378.
You have excellent interpersonal and communication skills and enjoy the exchange with internal and external stakeholders fluent in English and German.
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.
Please feel free to contact usYou 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.
Additional Information- Holistic corporate health management
- Flexible working hours
- Canteen
- Access to public transportation
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Quality Expert R&D and Global Engineering
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