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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

• Review and support in the Investigation of unconfirmed out of specification results.

• Investigating, reviewing and authorisation of Deviations, CAPAs in accordance with

• Participate in cross functional Pyramid Team meetings and support from a Quality

• Trending and analysing of quality data and contributing to the continued development of

• Conduct Self-Inspections and Site audit readiness inspections.

• Assisting in the approval of Standard Operating Procedures, Methods of Analysis,

• Preparation and Review of Finished Product Specifications and Shelf-Life Specifications

Essential Criteria:

Applicants must therefore demonstrate the following essential criteria on their application

form in order to be considered:

• A minimum of 2 years’ experience within a GMP/GLP laboratory setting.

• A minimum of 2 years’ experience supporting quality investigations.

• Excellent knowledge of GMP and Quality Management Systems.

• Excellent oral and written communications

Desirable Criteria:

Due to the nature of the role preference will be given to applicants demonstrating the

following desirable criteria:

• 3rd Level Qualification in Science / Pharmaceutical field.

• Experience with TrackWise including but not limited to raising deviations and CAPAs.

Duration: Full time, permanent

Location: Newry

Additional Information:

• This role will be based in a site that produces and handles penicillin, and as such, this

• Applicants should be able to provide proof that they have a right to work in the UK at the

• We regret that applications received after the closing date and time will not be accepted.

Benefits:

• Free Life Assurance • Employee Assistance Programme

• Company Pension Scheme • On-site free parking

• Healthcare cash plan • Canteen Facilities

• 32 days annual leave • Employee Perks scheme

• Wedding Leave • Employee Recognition scheme

• Company Sick Pay • Career development opportunities

• Employee well-being initiatives

Contact: recruitment@norbrook.co.uk

Norbrook Laboratories Limited employs a workforce with members of all sections of
the community and is committed to appointing people purely on the basis of merit. In
accordance with our equal opportunities policy, we would particularly like to welcome

applicants from the Protestant Community.