Scientist Ch

Role Overview

You will ensure the timely and cGMP-compliant execution of projects within your defined area of responsibility. This role requires strong organizational skills, attention to detail, and the ability to collaborate across multiple departments in a dynamic environment.

Key Responsibilities

• Act as interface to the analytics representative
• Approve corrections in ProNas and create label data
• Prepare projects (special materials for aliquoting, check packing lists, folders, etc.)
• Assist with and execute trainings
• Issue reserve and stability samples
• Order laboratory materials
• Ensure compliance with quality (SOP & GMP) and safety regulations

Cross-functional Interfaces

QC (Quality Control), QA (Quality Assurance), AD (Analytical Development), PD (Process Development), MSAT (Manufacturing Science and Technology), Operations, and Logistics

Your Profile

• Education/Experience: Minimum 1-2 years of experience in a GMP-regulated environment
• Languages: Fluent in English and German
• Technical Skills: QC software experience (LIMS, Trackwise) is a plus
• Strong organizational and communication skills
• Ability to work independently and in cross-functional teams

Why Join Us?

• Flexible work model (home-office possible)
• Opportunity to work in a cutting-edge life sciences environment
• Collaborative and supportive team culture