Job
- Level
- Experienced
- Job Field
- IT, Support
- Employment Type
- Full Time
- Contract Type
- Permanent employment
- Location
- Saarbrücken
- Working Model
- Onsite
Job Summary
In this role, you support production IT systems, optimize production processes, and document all activities according to GMP guidelines while closely collaborating with the central IT team.
Your role in the team
- Support and maintenance of production-related IT systems (OT systems) in close coordination with the central IT.
- Support in the establishment, validation, and documentation (CSV) of IT-supported production processes (GxP / GMP).
- Documentation of performed activities in the GMP-regulated OT environment in accordance with applicable SOPs, as well as support in validation and audits.
- Integration of production facilities and MES systems with higher-level systems in collaboration with IT and, if applicable, external partners.
- Analysis and resolution of hardware and software issues (1st and 2nd level), interface to central IT.
- Participation in the further development of existing applications and processes in coordination with specialist departments and central IT.
- Execution and documentation of activities in compliance with applicable IT, GMP, and safety regulations.
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Our expectations of you
Education
- Completed vocational training as an IT specialist (system integration or application development) or comparable.
Qualifications
- Knowledge of databases, operating systems, and IT system landscapes.
- Knowledge of systems such as Neuberger Particle Monitoring, Siemens Monitoring, JUMO, Promas, PAMS, or Smartcontrol is desirable.
- Analytical thinking, structured approach, problem-solving skills, meticulous and reliable work in a regulated environment.
- Very good spoken and written German skills, good English skills are an advantage.
Experience
- Professional experience in application support or IT support, ideally in a production environment within regulated industries (e.g., pharmaceuticals, chemicals, medical technology).
- Experience with production-related systems (e.g., monitoring, MES, or control systems) is an advantage.
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What we offer
- Crisis-proof and future-proof workplace in the growing pharmaceutical industry.
- Part of an innovative and modern family business.
- Varied activities and tasks in an exciting work environment.
- Comprehensive and thorough professional onboarding.
- Long-term perspectives and internal development opportunities.
- Attractive remuneration in accordance with the Chemical Industry Collective Agreement.
- Collaboration with motivated and professional colleagues.
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Topics that you deal with on the job
Job Locations
This is your employer
Ursapharm Arzneimittel GmbH
Since it was founded in 1974 URSAPHARM Arzneimittel GmbH has been developing new pharmaceutical concepts and translating them into successful medicinal products and medical devices for ophthalmology and general medicine. Today, URSAPHARM is a medium-sized, internationally operating company with its head office in south west of Germany.
Description
- Company Size
- 50-249 Employees
- Company Type
- Established Company
- Working Model
- Onsite
- Industry
- Pharmaceutical Sector, Chemical Industry, Biotech