• Company pension scheme with attractive employer contributions
• Modernly equipped workplaces in innovation centres
• Multiple training opportunities for your career
• Flexible working time models for a better work-life balance
• Discounted memberships to regional gyms
• Regular team events to strengthen your team
• Subsidised canteen with healthy food options
• Regular team events tobalance
• subsidised canteen with healthy food
• discounted memberships to regional gyms
• regular team events to strengthen team spirit

What you can always rely on at persona service:

• Intensive preparation for the interview with our client
• €50 per month as a gift for your mobility depending on the position, e.g. for a ticket to Germany and other benefits. e.g. for the Germany ticket and much more
• Bonuses as well as holiday and Christmas bonuses and attractive industry bonuses
• Free tutoring for your children on the Ubimaster learning and tutoring platform
• Numerous shopping discounts with well-known brands via our corporate benefits programme
• Excellent personal support and regular feedback meetings
• Multiple further training opportunities

• You will be responsible for independently managing and ensuring the GMP-compliant qualification of all equipment, rooms and technical systems in accordance with the applicable national and European guidelines
• In addition, you will be responsible for the professional review, continuous updating and final approval of relevant qualification documents and validation master plans, taking into account internal SOP specifications
• Furthermore, you will be responsible for process-related assurance, that only fully qualified and functional systems and equipment for the manufacture of pharmaceutical products are used at the site
• Your tasks also include defining and strategically developing site-related qualification standards according to the current state of the art and providing technical advice to the neighbouring specialist departments
• As part of your work, you will support the coaching of employees on GMP-compliant documentation and prepare and implement GMPcompliant documentation and create and maintain precise work instructions to ensure high quality standards
• In addition, you will actively support site-wide projects and PQR assessments and carry out the technical assessment of changes, which have a direct impact on the qualification status
• Finally, you are responsible for the technical lead function for qualifications and ensure compliance with global regulations on data integrity within the assigned areas of responsibility at the site

• You have successfully completed a degree in natural sciences with a Master of Science, Master of Engineering or Master of Pharmacy
• In addition, you have sound professional experience in the technical qualification of complex plants and systems within a highly regulated environment of modern pharmaceutical manufacturing
• You have a sound knowledge of the applicable GMP regulations and the specific requirements for data integrity.regulations and the specific requirements for data integrity make you particularly suitable for this responsible interface function
• You have a native level of written and spoken German and a good command of English, which you can use confidently for specialist documentation and communication
• In addition, you have a high level of organisational skills and a strong team spirit for successful collaboration with various internal and external specialist departments
• You have a good command of German and a good command of English, which you can use confidently for specialist documentation and communication. cooperation with various internal and external specialist departments
• Finally, you are characterised by your sense of responsibility and work with great initiative and technical interest in new issues of pharmaceutical quality assurance
• In addition to your technical expertise, you will also have a valid work permit and permanent residence in Germany to perform this responsible position