Job Description

Packaging QC - CAPA - SOP writing
Are you a hands-on QC analyst looking to grow your career in QA? Join a dynamic QC team in the pharmaceutical industry and contribute to maintaining reliable and compliant laboratory operations while supporting continuous improvement initiatives in the packaging unit.
Your main responsibilities

• Support QC compliance activities in line with cGMP and company quality standards
• Participate in internal and external audits and help implement resulting actions
• Coordinate and support change control assessments within QC
• Contribute to risk assessments and data integrity initiatives
• Bring your laboratory and process knowledge to ongoing QC projects
• Act as a key contact for systems such as LIMS and ERP, supporting users and coordinating small system improvements
• Participate in QC performance monitoring and help drive Lean initiatives (5S, Gemba, Pareto, Visual Management, etc.)

Your profile

• CFC or degree in life sciences
• 2-3 years of experience in a QC or GMP-regulated laboratory
• Good understanding of laboratory processes and analytical work
• Knowledge of QA processes and documents in QC
• Packaging Lab experience most welcome
• Strong organizational and communication skills
• Fluent in French, with basic English knowledge
• Team-oriented mindset and willingness to learn in a structured, process-driven environment

Why join

• Gain valuable experience with QA in a modern QC laboratory setting
• Work in a supportive team focused on compliance and improvement
• Take part in projects that shape the future of laboratory quality

gloor? AG
gloor? THE RIGHT CHOICE IN CONSULTATION FOR LIFE SCIENCE TALENTS

Skills Required