At a Glance
- Tasks: Lead quality investigations and implement corrective actions in a dynamic manufacturing environment.
- Company: Join a leading company committed to quality and continuous improvement.
- Benefits: Enjoy 32 days annual leave, healthcare cash plan, and career development opportunities.
- Other info: Exciting role with excellent perks and a supportive work culture.
- Why this job: Make a real impact on product quality and customer satisfaction in a vital industry.
- Qualifications: Third level qualification and 3 years' experience in a GMP or QC Micro role.
The predicted salary is between 37800 - 46200 £ per year.
Job ref: QAQCM260826
Job type: Permanent
Location: Newry
Closing date: Wednesday 09 Sep 2026 17:00
Job Overview
Reporting to the Head of QA/QC, based within the Quality Department, the successful candidate will be responsible for handling Micro quality investigations arising from identified deficiencies as reported from external and internal sources such as customer quality complaints, Out of Specification results, deviations etc. and for co-ordinating the implementation of corrective and preventative actions to address identified deficiencies. Working within the QA/QC team to implement Quality Management Systems and Continuous improvement projects within the manufacturing environment.
Main Activities/Tasks
- Investigating, Documenting, and Reporting of Customer Complaints, Deviations, OOS, CAPAs and other quality non-conformances.
- Participating, as a key contributor, in GMP audits by regulatory authorities and by contract customers and implementation of associated corrective and preventative actions.
- Working alongside Quality Control - Micro in the implementation, maintenance and improvement of the QMS within the QC environment.
- Trending and analysing of quality data and contributing to the continued development of the company and promoting all aspects of cGMP.
- Assisting in the approval of SOP's, PQRs and other quality documentation.
Essential Criteria:
- Minimum Education: Third level qualification.
- Minimum 3 years' experience within a GMP environment and or QC Microbiology role.
- Excellent knowledge of GMP and Quality Management Systems.
- Excellent oral and written communication skills.
Desirable Criteria:
- Experience in a Quality Assurance role.
- Knowledge of current regulatory requirements, in both the EU, and the US.
- Experience with solid dose manufacture.
- Experience with aseptic manufacturing.
Additional Information:
This role may be based in a site that produces and handles penicillin, and as such, this role would not be suitable for those that have a penicillin allergy. Applicants should be able to provide proof that they have a right to work in the UK at the time of their application. Applicants who are unable to provide this proof will not be considered. We regret that applications received after the closing date and time will not be accepted.
Benefits:
- Free life assurance
- Company pension scheme
- Healthcare cash plan
- 32 days annual leave
- Wedding leave
- Company sick pay
- Employee well-being initiatives
- Employee assistance programme
- Tech Purchase Scheme
- Salary sacrifice scheme
- On-site free parking
- Subsidised canteen facilities
- WeCare programme - supporting the local community
- Employee perks scheme
- Employee recognition scheme
- Career development opportunities
To Apply
Please forward your CV via the APPLY Now button below.
QA/QC Quality Manager employer: Norbrook
As a QA/QC Quality Manager in Newry, you will join a forward-thinking company that prioritises employee well-being and professional growth. With a comprehensive benefits package including a company pension scheme, healthcare cash plan, and generous annual leave, the work culture fosters collaboration and continuous improvement within a supportive environment. This role not only offers the chance to make a meaningful impact on quality management but also provides ample opportunities for career development and recognition.
