Your responsibilities: 

• Advice and support for projects with Corporate GxP-relevant computer systems and support the system owners of computer systems in life cycle management.
• Review of qualification/validation documents for new and existing GxP-relevant computerized systems, software and electronic equipment steering according to applicable cGxPs.
• Review and evaluation of change applications, deviations and related CAPAs concerning validation, qualification and life cycle management of computerized system and data integrity.
• Risk assessment and risk mitigation of computerized systems related to data integrity.

Your profile: 

• At least 5 years of experience in the validation of GxP-relevant IT systems such as ERP, LIMS, analytics systems or in process automation.
• Sound knowledge of cGxP requirements for pharmaceutical companies.
• Degree in sciences (MSc/BSc in e.g. computer science, chemistry, process engineering) or a science education with relevant professional experience. 

Your benefits: 

• A dynamic highly motivated work environment and a high value infrastructure.
• Possibility to enhance, increase and further develop you key competences.
• Option to work partly from home.
• 5 weeks holiday at minimum.
• contribution to children's day care. 
• Insurance covering private travels.
• Private accident insurance.
• 13th Salary, Social security to 100% covered by Carbogen Amcis.
• Bonus Program. 

Note for recruitment agencies: We do not accept unsolicited applications from recruitment agencies for this position. Unsolicited applications from recruitment agencies will be deleted and not be processed further. Thank you for your understanding.