In Norbrook we pride ourselves in being one of the top companies in Northern Ireland and
one of the top veterinary pharmaceutical companies globally. We develop & manufacture
veterinary medicines, supplying products to 120 countries globally. With a strong portfolio of
existing products and significant investment in R&D to launch new products annually, we
have opportunities for individuals to join us and develop their career in a global company.
Our business strategy is supported by our Values – Customer Value, One Team, Results
Driven, Excellence, Innovation, and Quality – and we support our employees to live the
behaviours that creates our culture. Our on-going success is based on the expertise,
knowledge and innovation of our employees. If you are interested in joining our team here at
Norbrook and supporting our vision, then apply for this role.
QA Associate – Pharmaceutical Development
Job Overview
Reporting to the Corporate QA Manager, based within the Quality Department, the successful
candidate will be responsible for reviewing, approving protocols / reports, Method of Analysis,
Standard Operating Procedures, handling of Out of Specification results, Deviations, co-
ordinating the implementation of corrective and preventative actions to address identified
deficiencies. Working within the site team to implement Quality Management Systems [QMS]
and Continuous improvement projects within the Pharmaceutical Development laboratory
environment.
Main Activities/Tasks:
- Working alongside Pharmaceutical Method Development, Stability, Regulatory and Site
QA in the implementation, maintenance and improvement of the QMS within the
Pharmaceutical laboratory environment.
- Review and support in the Investigation of unconfirmed out of specification results.
- Investigating, reviewing and authorisation of Deviations, CAPAs in accordance with
approved procedures.
- Participate in cross functional Pyramid Team meetings and support from a Quality
standpoint.
- Trending and analysing of quality data and contributing to the continued development of
the company and promoting all aspects of cGMP.
- Conduct Self-Inspections and Site audit readiness inspections.
- Assisting in the approval of Standard Operating Procedures, Methods of Analysis,
Protocols / reports and other quality documentation.
- Preparation and Review of Finished Product Specifications and Shelf-Life Specifications
against Registered Specifications.