QC Analyst - Day

Updated: April 13, 2024 08:20 PM GMT

Piramal Pharma Ltd

Falkirk

Job Description
• Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and
• stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good
• Documentation Practices for Electronic Data.
• Perform stability study programme activities, storage of in process, and final products samples and retention sample management
• System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department.
• Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents
• Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
• Checking and reviewing of data in compliance with Data Integrity requirements
• Actively... More Detail