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• Conducting, documenting, and evaluating complex (bio)analytical and analytical methods for IPC, release, and stability testing
• Optimizing and qualifying/validating (bio)analytical methods in a QC/GMP environment following handover from the development departments
• Preparing GMP-compliant documentation

QA Specialist (f/m/d) - CSV & QV In Bern, we're not just expanding-we're reaching a major milestone by launching a new production site and introducing innovative ways of working. This is what being a Persistent Pioneer in our BN DNA is all about-bringing a pioneering spirit to everything we do....

Lead Expert Quality Assurance, Deputy Responsible Person 40% Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing...

• Management of the QC department, including responsibility for budget and personnel
• Ensuring the timely QC testing of relevant materials (e.g., raw materials, intermediates, drug substances, finished drug products)
• Responsibility for method qualification/validation