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Job Details

QA Specialist – Leading Global Pharmaceutical firm – Ireland

Company: RBW Consulting
Location: IRELAND
Reference: AM-IRE-QS
Closing Date: 28 Oct 16
Type: Full Time
Salary (£): On Application
Benefits: Excellent, Full Benefits on Application

Job Summary:

An exciting opportunity has arisen for a highly motivated and organised individual to join my client, a leading global pharmaceutical firm as a QA Specialist. Working within their large Biologics division this position will join a dynamic team and be responsible for overseeing production within CMO’s.


The QA Specialist will be;

·         Reviewing batch documentation date, certificates of analysis and also provide support to the QP

·         Designing and implementing quality systems relating to batch disposition

·         Acting as lead auditor on an external basis

·         Supporting regulatory authority inspections

The ideal candidate for this position will be qualified to degree level or equivalent and possess a minimum of 2-3 years previous experience in a GMP environment. Any experience within Biologics would be hugely advantageous and the role will be based on site, in Dublin. In return this company can offer an excellent salary package to the right person along with strong opportunities for career progression.

Please contact me for further details.

Click here to apply for this job this position
At RBW Consulting LLP, every one of our consultants has the benefit of five years experience in helping Pharmaceutical Professionals find the jobs they are looking for in the industry.

With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for. Call +44 (0)1293 584 300 or email for a confidential discussion about your options for progression.

Keywords: CPM, Clinical, Antwerp, Brussels, Liege, Belgium, Holland, Netherlands, Programme, Program, Study, Studies, Trials, Matrix, International, CRO, Pharma, Pharmaceutical, Clinical Research Organisation, Organization, Targets, Target, Operations, Operational, Costing, Clinical Project Manager, Project Manager, Global Clinical Project Manager, Global Project Manager, PM, Operations Manager, Study Operations Manager, Study Manager, Clinical Study Manager, Global Study Manager, Global Study Operations Manager, Holland, Netherlands, CRA, Senior CRA, Lead CRA, Clinical Research Associate


Apply for this job: QA Specialist – Leading Global Pharmaceutical firm – Ireland

Contact Information:

Address:  Head Office
Origin Two 106 High Street, Crawley RH10 1BF
RH10 1BF
Tel:  01293 584 300
Fax:  01293 534 133
Website:  Visit Our Web Site

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