Manager CQV

Explore your tasks and responsibilities

• Responsibility for the personnel planning in the project
• Responsibility for the professional allocation of employees
• Instruction and further training of staff
• Cooperation in offer preparation
• Management and implementation of software validation and infrastructure qualification projects in the regulated life science environment
• Consulting, coaching and development of IT quality management concepts
• Introduction of CSV concepts into existing quality management systems (CSV policies, SOPs, validation master plans, etc.)
• Conducting workshops, GAP assessments and IT compliance audits as well as implementing and processing of CAPA plans
• Independent creation of life cycle validation and qualification documents for computer-aided or automated systems
• Validation and qualification of IT infrastructure and IT services as well as support in the acquisition of customer projects 

Show your expertise

• Completed academic training in natural sciences or engineering (computer science, automation technology, engineering, pharmaceutical technology or in a comparable field of study) 
• Very good of the underlying requirements (EU-GMP guidelines, 21 CFR Part 11/210/820, ISO13485, MDR etc.)
• Minimum 6 years of experience in the life science industry 
• Fluent use of both German and English is required 
• Proactive commitment to customers as well as a quality-oriented and independent way of working are self-evidently
• Willingness to work on-site with our clients 

Contact:

You want to be part of the Exyte team? We look forward to receiving your application!
For further questions and information, please do not hesitate to contact Ilayda Öztürk via E-Mail at [email protected].

Please note that we only consider applications submitted through our application portal. Applications sent via email will not be considered due to data protection regulations.