Description

In this role, you will be the go-to expert for GMP compliance, managing processes and supporting quality systems. Your day-to-day responsibilities will involve coordinating audits, optimizing compliance procedures, and fostering collaboration across teams and stakeholders.

Requirements

• •Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, or equivalent
• •Experience in synthetic and/or large molecule manufacturing and quality control
• •Flexibility and teamwork skills
• •Curiosity about team priorities and workload
• •Empowerment to make decisions and ownership of work
• •Seeking feedback for continuous improvement
• •Excellent language skills, fluent in German and good communication in English

Tasks

• •Manage local GMP compliance processes
• •Coordinate quality risk management activities
• •Facilitate handling of deviations and CAPA
• •Support changes in GMP compliance
• •Act as an expert for quality systems
• •Provide first-level support for business processes
• •Train subject matter experts on quality systems
• •Manage access to GMP relevant areas
• •Oversee account management for GMP systems
• •Handle inspection management for internal audits
• •Prepare for health authority inspections
• •Drive optimization of GMP-related processes
• •Standardize the existing document landscape
• •Collaborate with team members in a role-based environment
• •Build relationships with customers and partners