QC Lab Analyst x 2

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