25048_Analytical Study Manager (f/m/d) 100%

Published on: May 28, 2025

Job Description

Understand and cover the analytical aspects during the project development cycle for biologics (NBEs, biosimilars, ATMPs)
Act as interface between the operational teams and the dedicated project lead
Implement project plans with respect to customer expectations and requirements into operations and supervise project execution considering scope, quality, time and cost
Supervise cross-functional teams in a matrix setting
Preparation and management of project deliverables (protocols, reports, CoAs, etc)
Overlook compilation and review of analytical documentation
Perform risk analysis and support with quality event generation
Support and trigger troubleshooting activities

BSc or MSc in Life Sciences (e.g. Analytical Chemistry, Biochemistry, Biology, or Pharmacy), with at least 3 years of relevant industry experience in an analytical or development setting
Strong technical, organizational, and communication skills to collaborate effectively across cross-functional teams
Solid understanding of the pharmaceutical development process, both theoretical and practical
Experience with quality control standards
Proficient in English, both written and spoken; German is a plus
Familiarity with GMP guidelines and project management experience is a strong advantage

Our Offer

Comprehensive onboarding to ensure a smooth start
Flexible working models with a 40-hour work week and at least 28.5 vacation days annually
Diverse opportunities for professional development and career growth
Attractive pension plans and commuter subsidies for public transport users
Generous family benefits, including above-average child allowances and voluntary family support
Access to discounts via a voucher platform and subsidized Reka-Checks
An excellent on-site cafeteria