Quality Operations Specialist

3 weeks ago


Skipton North Yorkshire, United Kingdom Dechra Pharmaceuticals Limited Full time

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.
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
The Quality Operations Associate works closely with operational teams, quality control team, engineering team and other support function to ensure compliance to relevant SOPs and GMP standards and delivery of site quality metrics.
Plenty of training and development opportunities
~5 days annual leave + Bank holidays
~ Option to buy a week's holiday each year
~8% Employer Pension Contribution
~ Employee Assistance Programme
~ Discounted gym membership
~ Free on-site parking and electric charging

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
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
Review batch documentation for adherence to cGMP compliance.
Previous experience of working in a Quality environment and knowledge of document systems and indexing are desirable



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