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