Job
In dieser Position übernimmst du die Verantwortung für Siemens Opcenter Execution Pharma, koordinierst die Zusammenarbeit der Teams, planst und dokumentierst Computer System Validierung und sicherst die GMP-Konformität.
Deine Rolle im Team
- You take ownership of Siemens Opcenter Execution Pharma and work across sites with colleagues in Manufacturing, QA, IT/OT, and Process Control Systems (PLS).
- You bring together, assess, and prioritize system requirements with your stakeholders, keeping business needs in focus.
- Effective collaboration between PLS, MES, and IT/OT teams is in your hands: you bring the teams together and coordinate interfaces.
- You plan, manage, and document computer system qualification and validation (CSV) activities for the system and relevant changes.
- You keep GMP compliance at the heart of changes, releases, incidents, and deviations.
- Clear, up-to-date CSV, change management, and system documentation is part of your responsibility: you maintain it and develop it further.
- You help production teams rely on stable system operations that meet their needs, coordinating support, troubleshooting, and escalations with external providers.
- You manage the system lifecycle, changes, and releases and look after interfaces to PLS and other shopfloor systems.
Unsere Erwartungen an dich
Ausbildung
- You have a degree in automation engineering, electrical engineering, information technology, computer science, or a comparable qualification.
Qualifikationen
- You bring strong expertise in computer system qualification and validation and in preparing the relevant documentation.
- You understand how process control systems, MES, and other shopfloor systems connect and interact.
- Knowledge of Siemens Opcenter Execution Pharma is part of your technical profile.
- You work in a structured, independent, and solution-oriented way and enjoy bringing different stakeholders together.
- Your very good written and spoken German and English skills round off your profile.
Erfahrung
- You bring several years of experience with GMP-relevant manufacturing, shopfloor, or automation systems, ideally in a process control system environment.
- Experience in operating and supporting regulated systems, as well as managing their changes and lifecycle, defines your expertise.
Unser Angebot
- We ensure your financial stability with a competitive salary between 88.900€ and 108.000€ per year (full-time) plus a variable component.
- Your compensation is based on your qualifications, skills, and professional experience.
- Whether it's hybrid work models or part-time arrangements: Whenever it is possible, you will have the flexibility to work how, when and where it is best for you.
- Your family is a top priority. We offer loving company daycare centers at multiple locations, support in finding childcare, time off for the care of elderly or dependent family members, summer camps for children, and much more.
- We support your professional growth by providing access to learning and development opportunities, training programs through the Bayer Learning Academy, development dialogues, as well as coaching and mentoring programs.
- We promote health awareness and opportunities for selfcare through various measures, such as free health checks with the company doctor.
- We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work.
Benefits
Work-Life-Integration
Gesundheit, Fitness & Fun
Mehr Netto
Themen, mit denen du dich im Job beschäftigst
Job-Standorte
Das ist dein Arbeitgeber
Die Bayer AG ist ein international agierendes Unternehmen, das sich auf die Bereiche Gesundheit und Ernährung spezialisiert hat. Unser Fokus liegt auf der Entwicklung von Produkten und Dienstleistungen, um den Menschen und dem Planeten Gutes zu tun. Gemeinsam arbeiten wir an Lösungen, um den globalen Herausforderungen einer wachsenden und alternden Weltbevölkerung gerecht zu werden.
- Etablierte Firma
- Full Remote, Hybrid, Onsite
- Pharma, Chemie, Biotech
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