Quality Engineer - Pharma Solutions - Cork

Company: Confidential
Your Application: You have not applied yet
Location: Cork, Irlanda
JOB DESCRIPTION


Job Summary

BBBH787719
Jul 23,
Competitive

Excellent opportunity for a driven and passionate Quality Engineer to join a growing business. This is an all encompassing quality role giving you exposure to the full life cycle of the product

I currently am delighted to work with a fantastic company in who are experience an unprecedent growth spurt and due to this are on the look out for a Quality Engineer to join their team on a full time, basis. This is a great opportunity to join a business who is going from strength to strength and to join a highly passionate and inclusive Quality team.

The successful individual will be involved in the planning and conducting of activities concerned with the quality control and quality assurance of products manufactured in a cleanrooms environment

A bit more about the role.

Work as part of a value stream to ensure appropriate quality oversight and support to operations
Drive continuous improvement and embed a culture of quality to ensure ongoing compliance with relevant regulations ISO 9001
Troubleshoot complex problems as part of a cross functional value stream
Ensure the QMS is in place, in use and aligned to current regulatory expectations
Design and implement test plans and audits for products to ensure product quality targets are met
Establish, define, implement, maintain, and report on quality assurance key performance measures and standards
Investigate non-conformances and consumer complaints, perform root cause analysis, implement corrective actions, and monitor progress and improvements
Create and maintain quality systems documentation, such as quality manuals, procedures, and work instructions
Perform quality assurance and qualification audits on vendors/suppliers

Participate in and host customer audits of the facility
Devise sampling procedures, design and develop forms and instructions for recording, evaluating, and reporting quality data
Write technical reports
Coach and support others in relation to quality Confidential practices as required

Qualifications and Experience:

Bachelor of degree in Engineering, Science or equivalent
5 - years of experience working in a regulated environment ISO accredited, Pharmaceutical, medical devices etc.
Familiarity with cleanroom manufacturing
Working knowledge of Confidential Office applications
Experience in general quality systems internal and external audits, CAPA management, customer complaints handling, non-conformance management etc.
Ability to articulate complex problems in a clear concise manner through effective communications and technical report writing skills
Strong analytical problem solving skills
Demonstrated ability to work collaboratively as part of a cross functional team
Ability to communicate effectively at all levels of the organisation

, or if you would like to find out more, reach out to Kellie O'Donovan today on 2300 or kodonovanmorganmckinley

Confidential is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF Confidential SERVICES.

Apply Now
Consultant Details
Consultant Details
Kellie O'Donovan
Senior Consultant | Engineering Recruitment - Quality & Validation

0 2300300

kodonovanmorganmckinley



JOB TYPE
Work Day: Full Time
Employment type: Permanent Job
Salary: Negotiable


JOB REQUIREMENTS
Minimal experience: No experience



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