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
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