QA Document Controller - Cork

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


Job Summary

BBBH788569
Jul 26,
Competitive

The perfect opportunity for a QA Specialist who wants to move out of operations, or a experienced doc controller to join a unique and passionate company

I currently am delighted to be working with an exciting and innovative US based company who are looking to invest even further into their Irish operations. This company are a market leader and are hugely passionate about investing in their people and their products. They are currently on the lookout for a QA Document controller to join their team on a basis.

The Document controller will report to the QA Manager and will be involved in creating manufacturing and production records and overseeing document reviews to ensure compliance with quality standards.

You will;

Assists in audits.
Develop and create quality procedures and documents and coordinate with manufacturing personnel.
Communicates deviations to Quality Management and assists in CAPA & complaint investigations.

A bit more about the role;

Maintain and update deviation and Material Review Board processes.
Performs batch record review and approval as outlined to product specification.
Responsible for performing release or reject activities in SAP.
Assists with the development of procedures and forms.
Responsible for reviewing documents for incoming raw materials/Components
Collaboration with Document Control counterparts in Global HQ.
Collates data to report weekly metrics to QA Workgroup and daily to site workgroup.
Active participant in the site CI program.

What do you need to have;

2-5 years of QA/ Doc control experience in a regulated food or pharmaceutical facility
Bachelor's degree in a science related discipline preferred.
Internal auditing qualification advantageous.
Strong attention to detail.
Excellent communication skills, interpersonal skills and problem-solving skills.
Strong organisational abilities, must be self-motivated and display an ability to meet deadlines.
Working knowledge of automated doc control systems, data entry and Confidential Office suite required.
Self-starter and ability to adapt to changing priorities.
Knowledge and experience with applicable FDA and other regulations and cGMP requirements.
Knowledge of SAP would be highly advantageous.

, 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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