Quality Operations Associate (lates)

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

The Opportunity

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.

Role Responsibility

So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:

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.

The Ideal Candidate

Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We’re particularly keen to hear from those who have/are:

Must have previous experience of working in a GMP manufacturing environment
Experience and ability to drive issues through to a satisfactory conclusion
Previous experience of working in a Quality environment and knowledge of document systems and indexing are desirable

Due to the nature of our business, all successful candidates must complete a basic DBS check (Disclosure and Barring Service check) before employment can commence, and at regular intervals during employment. Dechra will pay for this check.’

Package Description

Average 36-hour working week (with a day off every other Friday!!)
Lates, 1400-2230
Plenty of training and development opportunities
22.5 days annual leave + Bank holidays
Option to buy a week's holiday each year
8% Employer Pension Contribution
Free access to the Headspace App
Employee Assistance Programme
Discounted gym membership
Free on-site parking and electric charging