Job
In this role, you take responsibility for Siemens Opcenter Execution Pharma, ensure system qualification, and collaborate closely with Production and IT/OT to ensure smooth interface coordination.
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Your role in the team
- You will take on system responsibility for Siemens Opcenter Execution Pharma and work across sites with colleagues from Production, QA, IT/OT, and process control systems (PCS).
- You gather, assess, and prioritize system requirements together with your stakeholders while keeping operational needs in mind.
- Effective collaboration between PLS, MES, and IT/OT teams is in your hands: You bring the teams together and coordinate the interfaces.
- You plan, manage, and document the qualification and validation of computerised systems (CSV) for the system and relevant changes.
- You put GMP compliance at the center of changes, releases, incidents, and deviations.
- Maintaining and continuously improving clear, up-to-date CSV, change management, and system documentation is part of your responsibilities.
- You help production teams rely on stable, demand-driven system operations and coordinate support, incident resolution, and escalations with external providers.
- You manage the system lifecycle, changes, and releases, and oversee the interfaces with PLS and other shop-floor systems.
Our expectations of you
Education
- You have completed a degree in automation engineering, electrical engineering, information technology, or computer science, or have an equivalent qualification.
Qualifications
- You have in-depth knowledge of the qualification and validation of computerised systems, as well as experience preparing the relevant documentation.
- You have a very good understanding of how process control systems, MES, and other shop floor systems are connected and work together.
- Knowledge of Siemens Opcenter Execution Pharma is part of your professional skill set.
- You work in a structured, independent, and solution-oriented manner, and enjoy bringing different stakeholders together.
- Your excellent written and spoken German and English skills round out your profile.
Experience
- You have several years of experience with GMP-relevant production, shop floor, or automation systems, ideally in a process control system environment.
- You have experience operating and supporting regulated systems, as well as in change and lifecycle management.
What we offer
- We ensure your financial stability with an attractive annual salary of €88,900 to €108,000 (full-time), plus a variable component.
- Your compensation is based on your qualifications, skills, and professional experience.
- Whether it’s hybrid working or part-time: whenever possible, we give you the flexibility to work how, where, and when works best for you.
- Your family comes first: We offer caring company daycare centers at many locations, support in finding childcare, leave to care for family members, holiday programs, and much more.
- We support your professional development by providing access to learning and development initiatives, courses and training through the Bayer Learning Academy, development discussions, as well as coaching and mentoring programs.
- We support your health and a self-care-oriented lifestyle through a range of initiatives, including free health checks with the company doctor and health seminars.
- We celebrate diversity in an inclusive work environment where you are welcomed, supported, and encouraged to bring your whole self to work.
Benefits
Work-Life-Integration
Health, fitness & fun
Higher take-home pay
Topics you will work on
Job locations
About your employer
Bayer AG is a globally active company with core competencies in the life science fields of health and nutrition. We develop our products and services for the benefit of people and the planet, and are committed to addressing the global challenges of a constantly growing and aging world population.
- Established Company
- Full Remote, Hybrid, Onsite
- Pharmaceutical Sector, Chemical Industry, Biotech
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