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.
Regulatory Manager • Jülich (DASGIP)