QC Analyst

Waterford  ‐ Onsite
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Keywords

Description

One of our clients based in Waterford have an opening for a Quality Control Analyst on a 6 month contract.This is an exciting opportunity to work with one of the leading pharmaceutical global firms. This role is an initial 6 month hourly rate contract position with the possibility of a further extensions.

Scope of Responsibility: -
* Permit and Promote only desirable activities and behaviours. * Sampling and testing activities carried out for the specified QC team in line with GLP and business targets.
* Achieves Lead-time targets (and proactively addresses barriers to achievement)
* Ensures full ESH compliance in QC activities
* Ensures full GLP compliance in QC activities
* Ensures QC documentation and LIMS relating to team activities is in compliance.
* Facilitates improvements in QC processes
* Meets CAPA and other site metrics
* Completes On-The-Job Training process & training record
* Supports PPR and other site processes
* Supports site OE projects (specifically JDI and lab efficiency)

Impact of role on business objectives: -
* Ensure QC team work in a safe manner and in accordance with GxP
* Training of QC team for specific tasks in accordance with GxP
* Decision-making and liaison with internal departments in order to gather information in order to disposition product in accordance with GMP
* Liaison with corporate colleagues as required to resolve issues
* Highlighting issues to the Quality Control Manager, OQ Manager and Quality Director as appropriate
* Reviewing completed analytical reports prior to OQ approval.
* Preparation and review of in-house procedures (SOPs)
* Troubleshooting analytical problems
* Scheduling in-house functions to ensure that the QC team operates as efficiently as possible and that product leadtimes are maintained.
* Provide support to site OE projects.

Basic qualifications:-
- Educated to primary or higher degree level-Chemistry or associated science
- Expected level of application of Knowledge
* Third level science-based degree.
* 2-3 years experience in a pharmaceutical / healthcare industry.
* Understanding of appropriate Directives, Standards, Quality Managements Systems related to the manufacture of Medical Device and Medicinal for required markets.

If you feel that you would be a good fit for this role please apply to this advert or contact me Derek Sheridan directly on for further information.

To find out more about Real please visit www.realstaffing.com
Start date
06/2013
Duration
6 months
From
Real Staffing
Published at
08.06.2013
Project ID:
548664
Contract type
Freelance
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