QC Lab Specialist
Industry : Pharmaceutical
Role Description:
The QC Analyst will be responsible for coordinating and/or performing all laboratory activities including but not limited to:
- Have an understanding and competence in GLP and laboratory workflows.
- Perform sampling, testing, release and investigation activities associated with materials in accordance with cGMP requirements.
- Perform analytical testing including preparation and review of documentation and any investigations for in process and finished combination products in accordance with cGMP requirements.
- Perform analytical testing and any investigations with external test laboratories to ensure compliance to cGMP requirements.
- Support lab support activities (Sample Management, Chemical / Consumables management, Specification / Method management, Equipment Management) to ensure compliance with local procedures and GLP requirements.
Qualification and Experience:
- Must have minimum of Level 8 qualification in scientific discipline.
- 2 – 3 years’ experience in Pharmaceutical QC testing Laboratory is required.
- Experience with testing of devices / combination products / inhalation testing is preferred.
Skills:
- Demonstrated understanding of pharmaceutical QC laboratory operations and GLP.
- Excellent communication skills must be able to comprehend and follow written and verbal procedures or instructions.
- Must be able to work flexible schedules as required to support lab & production activity.
- Proven ability to work cross functionally and within teams.
Duration: Permanent role with 6 months probation.
Location: Tipperary
To apply for this job email your details to enquiries@qaresources.com.