Lead projects in pharmaceutical analytics and ensure efficient execution in a hybrid working environment in Germany.
Responsibilities
Lead projects in the field of pharmaceutical analytics
Plan and monitor the execution of pharmaceutical projects
Organize and coordinate the project team
Ensure technically sound, on-time and cost-efficient project delivery
International project-related customer contact, possibly with a regional focus
Support customer and regulatory audits (GMP, FDA inspections)
Prepare and approve cross-functional documents, such as SOPs, test specifications, plans and reports
Requirements
Completed degree in a natural science (Master’s/Diploma or PhD in Biochemistry, Biology) or extensive professional experience in pharmaceutical analytics
Several years of hands-on laboratory experience working with cell cultures
Advanced user skills in MS Office, especially Word and Excel
GMP knowledge is desirable
Strong interpersonal skills and ability to communicate actively in German and English
Occasional travel within Europe (primarily Benelux countries)
Customer-oriented and quality-focused working style
Benefits
Flexible working hours with a flexitime arrangement (full-time 37.5 hours per week) and 30 days of annual leave
Mobile working 1–2 days per week by arrangement
Comprehensive onboarding as well as individual training and development opportunities with career prospects within a global corporate structure
Flat hierarchies and an informal, first-name culture ("Du"-culture)
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