- Create and update Validation Manuals (IQ & OQ) and procedures for the new releases of Mettler-Toledo software products suitable for regulated market.
- Produce high-quality documentation that meets applicable standards and is appropriate for its intended audience.
- Cooperation with Requirement Engineer to provide input regarding the regulated functionalities to R&D,
- Research and gather information on the regulations which apply or may apply in regulated industry beside computerized systems to specify the most suitable requirements,
- Give CSV Training classes, create validation eLearnings and support the validation of computerized systems (based on our system solutions).
- Minimum 1 year of experience in IT and Software Validation (CSV, GAMP5), preferably in pharma environment,
- Proficiency in spoken and written English,
- Knowledge of FDA 21 CFR Part 11, EU Annex 11 and GxP practices,
- Ability to quickly grasp complex technical concepts and make them easily understandable in text and pictures and clear for others,
- Willingness to work with documentation and analytical thinking,
- Very good communication skills.
- Stable employment conditions based on the contract of employment (umowa o pracę).
- Annual bonus.
- IP rights.
- Hybrid mode of work.
- Medical care with a basic dental package.
- Life insurance.
- Sport card and benefit platform.
- Language courses.
- An interesting and challenging career in a successful leading global organization.
- Possibility to work in an international environment with a multicultural team.
For those who prioritize precision, Mettler Toledo is precisely where you belong.
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Legal Entity