Meet Tine Holland Frimann. Tine is GMP Area Specialist in our Quality & Regulatory affairs department. The department covers quality control, quality assurance and regulatory affairs.
The department analyse all critical raw materials, do in-process controls and analyse the finished products to ensure that our products are always within specifications. They also support our customers with requested documentation, host audits and support the customer’s needs for registration of APIs with the authorities.
At Novo Nordisk Pharmatech we keep the quality management system up-to-date making sure we are in compliance with the requirements set to us.