Quality Technician
- Employer
- Manpower Ireland
- Location
- Dublin
- Salary
- Negotiable
- Closing date
- 24 May 2018
View more
- Sector
- Manufacturing
- Job Type
- Permanent
- Hours
- Full-time
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Quality Technician required to complete and support activities within the Quality Department relating to GMP Compliance and raw material/product release. To provide Quality support for the manufacturing operations.
Key Responsibilities
Daily briefing on Quality batch review/approval
Provide quality performance information as required
Ensure regular Quality interaction with other Departments
Material release - testing of raw materials and ID testing finished product
Sampling of raw materials/packaging
Quality batch documentation review and control
Quality in-process control including vial defect inspection
Customer complaint investigation
Annual product quality reviews
Support the process change control system
Support the quality audit/inspection programmes
Process/product/system improvement projects
Provide Quality input to process/product investigations (including planned / unplanned deviation)
Provide information to Regulatory Affairs as required
Training of new Quality personnel where appropriate
Review of Batch Records and SOPs
GMP implementation and site-wide Quality Awareness.
Follow up corrective actions identified through the Deviation system.
Liaise with other Department representatives to promote improvements in GMP and Quality standards.
Keep abreast of the latest developments from regulatory authorities in relation to Quality Compliance activities.
Applicants should have a Minimum of B.Sc Degree or equivalent third level education and at least 2 years experience in a quality or production function within the pharmaceutical industry.Excellent communication skills required.
Competence in Microsoft packages specifically word, excel and PowerPoint
Good organizational skills and flexibility required
This job would suit a results orientated individual.
Contact Ann Marie Corcoran for more information
Key Responsibilities
Daily briefing on Quality batch review/approval
Provide quality performance information as required
Ensure regular Quality interaction with other Departments
Material release - testing of raw materials and ID testing finished product
Sampling of raw materials/packaging
Quality batch documentation review and control
Quality in-process control including vial defect inspection
Customer complaint investigation
Annual product quality reviews
Support the process change control system
Support the quality audit/inspection programmes
Process/product/system improvement projects
Provide Quality input to process/product investigations (including planned / unplanned deviation)
Provide information to Regulatory Affairs as required
Training of new Quality personnel where appropriate
Review of Batch Records and SOPs
GMP implementation and site-wide Quality Awareness.
Follow up corrective actions identified through the Deviation system.
Liaise with other Department representatives to promote improvements in GMP and Quality standards.
Keep abreast of the latest developments from regulatory authorities in relation to Quality Compliance activities.
Applicants should have a Minimum of B.Sc Degree or equivalent third level education and at least 2 years experience in a quality or production function within the pharmaceutical industry.Excellent communication skills required.
Competence in Microsoft packages specifically word, excel and PowerPoint
Good organizational skills and flexibility required
This job would suit a results orientated individual.
Contact Ann Marie Corcoran for more information
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