Midas Pharma GmbH | Germany | 55xxx Ingelheim | Permanent position | Full time | Published since: 23.07.2026 on stepstone.de
Quality Assurance Manager Computer System Validation (CSV) (m/f/d)
Where people make the difference
The working day at Midas Pharma is varied and challenging. This challenge motivates and inspires us. This is also reflected in the people who work here: our employees make the difference.
We know: In the team we achieve more. This is how knowledge transfer works, only so we create the synergies that make us so successful as a company. This is why teamwork is self-evident. For our employees, this means: here there are spaces to move and take responsibility. Commitment, expertise and creativity meet flat hierarchies, short decision-making and highly-competent colleagues. An inspiring environment that motivates you to go one step further. Working for our customers and developing their own skills.
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Your tasks • Your profile • What we offer
Where people make the difference
The working day at Midas Pharma is varied and challenging. This challenge motivates and inspires us. This is also reflected in the people who work here: our employees make the difference.
We know: In the team we achieve more. This is how knowledge transfer works, only so we create the synergies that make us so successful as a company. This is why teamwork is self-evident. For our employees, this means: here there are spaces to move and take responsibility. Commitment, expertise and creativity meet flat hierarchies, short decision-making and highly-competent colleagues. An inspiring environment that motivates you to go one step further. Working for our customers and developing their own skills.
Planning, coordination and implementation of the validation of computer-assisted systems in accordance with applicable regulations Ensure compliance with legal requirements during all phases of validation of computer-assisted systems Management of all documents related to validation projects Implementation of risk management in the context of computer validation (CSV) Ensuring data and system security First contact for all questions related to validation processes Planning, supervision and supervision of validation, qualification and calibration measures Support of computer-assisted systems over their life cycle incl. Performing Periodic Reviews Coordination and processing of deviations and changes Creation and review of GMP-related documents
Complete study of computer science or natural sciences as well as several years of professional experience in the quality management of the pharmaceutical industryFunded knowledge in the validation of computer-assisted systems in the pharmaceutical industryYou are familiar with the current GMP requirements and guidelines for the validation of computer systems (GAMP5)High organisational capacity, result-oriented functioning and rapid adaptabilityGood communication skills, joy interdisciplinary workVery good German and English skills
A job in an established and prestigious family business, which offers you a personal and value-assurance working environment in addition to the safety of more than 35 financial years.A modern working environmentOverviewable benefits such as JobRad, EGYM Wellpass, employees’ restaurant, regular events and more.We have made a clear choice for small groups to promote a clear hierarchy.
Location
![]() | Midas Pharma GmbH | |
| 55218 Ingelheim | ||
| Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
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