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Quality officer - heywood

Heywood
Neogen
Quality officer
Posted: 1 July
Offer description

It's fun to work in a company where people truly believe in what they are doing!

The Quality Systems Officer will be responsible for ensuring quality activities meet with organizational requirements for quality management, health & safety, legal stipulations, and environmental policies.

The job holder has full responsibility for:
1.Ensure Quality standards are maintained and QMS procedures are followed correctly.
2.Maintain systems for measuring necessary aspects of quality management and regulatory.
3.Monitor, measure and report on quality issues, opportunities and risks within agreed formats and timescales.
4.Ensure quality activities meet with organizational requirements for quality management, health & safety, legal stipulations, and environmental policies.

It's fun to work in a company where people truly believe in what they are doing!

We are currently looking to recruit a Quality Officer to join our award-winning business. This role is based on-site in Heywood.


The Quality Officer is responsible for ensuring quality activities meet with organizational requirements for quality management, health & safety, legal stipulations, and environmental policies. This includes ensuring Quality standards are maintained and QMS procedures are followed correctly, maintaining systems for measuring necessary aspects of quality management and regulatory, monitoring and reporting on quality issues and ensuring quality activities meet with organizational requirements for quality management.

What you’ll be doing:

1. Perform and maintain core site activities of the QMS including document control, CAPAs, Investigations, Complaints, Supplier Management and Change controls.
2. Ensure corrective actions are taken to address non-conformances and perform verifications.
3. Undertake detailed root cause analysis and identify opportunities for improvement.
4. Perform process internal audits in adherence to audit schedule.
5. Maintain KPIs from electronic QMS activities weekly/monthly and provide detailed trend analysis of non-conformities.
6. Responsible for Quality Induction and eQMS training.
7. Responsible for label updates and final approval of product labels.
8. Support the company certification to ISO9001, ISO13485 and ISO17025 accreditation. Support the preparation and facilitation of client/regulatory audits.

About you:

9. Relevant scientific qualification desirable, but not essential.
10. Previous experience within QA is desirable.
11. Previous experience with electronic Quality Management Systems, but not essential.
12. Excellent interpersonal and communication skills.
13. Computer literate (Microsoft office packages such as outlook, word, excel) and good administrative skills with extensive experience of report writing.
14. Methodical, process driven with a high attention to detail.
15. Ability to work to deadlines while producing work of a high standard and accuracy.
16. Ability to prioritize and manage own workload.

Please press Apply now in order to submit your application.

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