Would you like to work for a company who has made it its mission to make a contribution to improving human living conditions? With around 5,000 employees worldwide Eppendorf is a leading Life Sciences company. We develop and distribute devices, consumables and services for use in laboratories worldwide. Our daily work is characterized by our principle: Collaborate on new ideas. You would like to take responsibility and help to make a difference in an experienced international company? Exciting tasks combined with a positive and affirmative working environment await you at Eppendorf. You are also motivated by technical challenges? Then apply now!

Your challenges

• Author, own and maintain internal guidance and training documentation

• Collaborate with various functions within the global company, internal and external suppliers and with customers with the objective to share expertise and provide guidance

• Review documents to ensure alignment regarding GMP customer expectations and suitability in the framework of GMP guidelines

• Provide target group specific trainings and participate in global broadcast presentations

• Close collaboration with the Quality team to align on concept and proper application of existing quality systems and support their development

• Providing active support to colleagues in implementing requirements and translate them into solutions

Your expertise

• Degree (Bachelor, Master, PhD) in the field of natural science, biotechnology or comparable

• Solid quality background, specifically with core GxP systems like Change Control, Deviation Management, CAPA

• Professional experience in quality or regulatory in manufacturing pharma industry, CMO/CDO/CDMO companies or in industry developing, manufacturing, and marketing of equipment for use in pharmaceutical manufacturing

• Professional experience with specific quality tools used in pharmaceutical industry like: Computer software validation (CSV) based on the principles of e.g. 21CFR11, Equipment qualification (IQ/OQ) Eurdalex Vol 4 Annex 15, Process Validation, Extractable / Leachable data generation and evaluation, Critical impurities and contact material compliance (e.g. TSE)

• Excellent communication skills in German and English in spoken and writing

• Accurate and detail-oriented mindset

• Highly skilled in standard Microsoft Office applications

• Passionate and motivating attitude

Your benefits at Eppendorf

• Your work is meaningful. Together we contribute to improve human living conditions.

• We offer you creative freedom with a strong, international premium brand in the life science industry.
• Thirty vacation days per year and company-regulated special leave days are a given with us.
• With our flexible flextime framework and a working time account, you can plan your working hours individually and independently create a balanced work-life balance.
• We also offer you the opportunity to work remotely across Germany for part of your working time, tailored to suit your life situation.
• We provide you with a variety of social benefits, such as additional employer-funded retirement plans, a job bike, public transport subsidies, corporate benefits, etc.
• To deepen your knowledge and continuously develop professionally and personally, we offer you a wide range of freely selectable training sessions, participation in conferences, and access to learning platforms.
• With us, you will find a diverse, open-minded, and appreciative work environment with the latest technologies, methods, and tools in a set

Please note that we can only consider applications that are submitted online via our application management tool.

We look forward to meet you!

If you have any questions please contact:

Mechthild Lautenschläger,

lautenschlaeger.m@eppendorf.de

Eppendorf. Collaborate on new ideas.