Senior Analytical Specialist – QC Method Compliance

Role Overview

• Support analytical method validation, method transfer and method comparison activities in collaboration with SMEs
• Coordinate validation and transfer activities including planning, documentation, data evaluation and reporting according to GMP requirements
• Prepare, review and maintain validation documentation, Master Methods of Analysis and product specifications
• Support troubleshooting and investigation activities together with global QC stakeholders
• Manage and maintain QC-related databases and corporate document management systems (e.g. Veeva)
• Coordinate reference material calibration activities including documentation and stability verification

Requirements

• Degree in Life Sciences, Chemistry, Pharmacy or a related field
• Experience in Quality Control within the pharmaceutical industry
• Good understanding of GMP requirements and analytical data evaluation
• Strong organizational, communication and project management skills
• Confident handling of MS Office and data/documentation systems
• Fluent English skills

Benefits

• Company restaurant & meal subsidy
• Training & further education
• Health promotion
• Parking spaces and good public transport connections
• Company and team events