Divisional Quality Governance Lead

6 days ago


Northwich, Cheshire, United Kingdom Dechra Pharmaceuticals PLC Full time

About Dechra Pharmaceuticals PLC

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We are a global specialist in veterinary pharmaceuticals and related products business.

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Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.

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The purpose of this role is to develop, implement, maintain, and continuously improve Dechra Group and DM&S Divisional Quality Management System processes and procedures that will create an acceptable baseline level of quality and GMDP control across different sites and business units, drive quality improvement, and increase operational efficiency.

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This includes creating, implementing, and maintaining procedures and guidelines related to Dechra's QMS at a divisional level (specifically Change Control, Deviation, CAPA, and Continuous Improvement), ensuring Quality Risk Management is implemented across GMDP areas of the business via the Group Quality Documents framework in accordance with ICHQ9(R1), and managing the Quality Risk Register (QRR) process for GMDP operations.

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The salary for this role is estimated to be around £60,000 - £80,000 per annum, depending on experience.

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About the Role

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  • ">
  • Create and implement divisional-level quality management system processes and procedures.">
  • Develop and manage quality risk registers and ensure compliance with relevant regulatory guidelines.">
  • Work closely with internal teams to identify and mitigate quality risks.">
  • Lead quality assurance activities and implement continuous improvement initiatives.">
  • Provide guidance and support to employees on quality-related matters.">
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About the Company

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Dechra Pharmaceuticals PLC is a global leader in veterinary endocrinology and topical dermatology, with a broad portfolio of analgesia, anaesthetics, and products for the treatment of pain.

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We deliver high-quality products and services to veterinarians worldwide through our employees and a network of third-party providers.

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Suitable candidates will have significant experience in the pharmaceutical industry, preferably in the veterinary pharmaceutical sector, and a strong understanding of relevant regulatory authority guidelines, including UK/EU/US GMPs and GDPs and ICH 10.

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They will also possess excellent verbal, written, and interpersonal communication skills in English.

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Please note that occasional global travel may be required for this role.



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