Quality Operations Associate (earlies)

at  Dechra Pharmaceuticals PLC

Job Introduction
Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra Pharmaceuticals PLC.
Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.
Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2000 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business

• Perform in process-checks to ensure Quality based systems and procedures are followed within the operations functions. Makes decisions and recommendations on actions needed to resolve technical and GMP compliance issues
• Provide guidance on operational changes and improvements
• Support internal and external quality/technical audits
• Training of new team members. Provide technical training on current and emerging regulatory requirements
• Actively aid in the delivery of the QA KPI’s
• To be located in operations and ensure that GMP, Quality, batch specific and (where applicable) client requirements are being adhered to at all times within the Operations area
• Participate in CI activities and projects through challenging current working practices with a view of improving efficiencies and Quality standards
• Prioritise workload and ensure key quality issues and business priorities are addressed and escalated appropriately and resolved in a timely manner
• Assist in quality investigations and participate in incident meetings
• Verify cGMP data entries into site computer systems
• Participate in required site meetings as representatives of Quality when required
• Apply problem solving capabilities to determine root causes of issues and identify effective CAPA to increase right first time and improve efficiencies and reduce operating costs
• Review batch documentation for adherence to cGMP compliance