Product Lifecycle Engineer (m/w/d)

Job title:

Product Lifecycle Engineer (m/w/d)

Company

Schott Pharma

Job description

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 usHuman 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. In light of this spirit, SCHOTT Pharma is committed to sustainable development for society and the environment and has the strategic goal of becoming climate-neutral by 2030.Your ContributionYou are an optimizer and innovator – analyzing a fast growing pharma packaging portfolio for optimization potentials with an interdisciplinary team, finding innovative solutionsYou are a task manager – planning and managing tasks to maintain our products compliant and competitive, collaborating in an international environment, communicating to various management levelsYou are an experienced technical writer – defining task-tailored documentation strategies with a strong focus on a risk based approachYour ProfileUniversity degree in Engineering, Life Science or similar3+ years of working experience in product development of medical devices, pharmaceutical packaging or similarExperienced with documentation in highly regulated environmentAbility to plan, manage and execute lifecycle and validation tasks in self-reliant mannerGood technical and analytical skillsGood interpersonal and communication skills with internal and external stakeholdersFluency in English and German (written and spoken)Your BenefitsSCHOTT’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; Exclusive employee benefits/discounts; Holistic corporate health management; Team EventsPlease 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.Your ContributionYou are an optimizer and innovator – analyzing a fast growing pharma packaging portfolio for optimization potentials with an interdisciplinary team, finding innovative solutionsYou are a task manager – planning and managing tasks to maintain our products compliant and competitive, collaborating in an international environment, communicating to various management levelsYou are an experienced technical writer – defining task-tailored documentation strategies with a strong focus on a risk based approachYour ProfileUniversity degree in Engineering, Life Science or similar3+ years of working experience in product development of medical devices, pharmaceutical packaging or similarExperienced with documentation in highly regulated environmentAbility to plan, manage and execute lifecycle and validation tasks in self-reliant mannerGood technical and analytical skillsGood interpersonal and communication skills with internal and external stakeholdersFluency in English and German (written and spoken)

Expected salary

Location

Saint-Gall

Job date

Sun, 29 Jun 2025 02:59:13 GMT

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