Overview

Team Lead Facilitator QC required by our client a leading pharmaceutical company based in Waterford City. The Team Lead Facilitator QC person will the Quality  team on a Full Time, Permanent basis in Waterford.. This role is based on a 2 shift cycle – Day shift 6am – 2pm & Evening shift 2pm – 10pm

Key Responsibilities of the role:

  • To Facilitate and lead the QC team to achieve agreed customer service levels
  • Deliver Customer Service level of >95% by testing components/raw materials/finished product/stability samples in an efficient and timely manner
  • Provide coaching, feedback and ongoing support to team members to ensure they have the necessary skills to perform their duties to the required standards
  • Review work schedule in advance to ensure all relevant components and equipment are available
  • Prioritise daily work schedule to ensure effective analysis of product and adherence to Operational schedule and Stability program timelines as required
  • Plan and organise calibration, maintenance and validation of instruments as required
  • Select and assign people to specific projects and tasks
  • Ensure that all QC documentation is completed correctly and right first time
  • Investigate and authorise Out of Specification investigations with QC Analysts
  • Issue and control of worksheets
  • Perform a detailed review of all analytical data generated in QC on raw materials, and finished products as required to meet the production schedule

The ideal candidate will be  

  • Degree level educated within a scientific discipline  
  • Have a knowledge of cGMP, and GMP for Labs requirements.            
  • Broad Knowledge of Analytical Techniques and Experience in HPLC/UPLC
  • A min of 2 years People management experience
  • Experience in Calibration Systems
  • Operation of Laboratory Instruments skills
  • Experience of Chemicals and Associated Dangers
  • Knowledge of Company Policies, Procedures and Quality Systems     
  • cGMP Regulatory Bodies Experience
  • Knowledge & Understanding of the Chemical / Pharmaceutical Manufacturing sector
  • Familiarity with US and European regulatory guidelines.
  • Documentation Compliance experience
  • Report Writing / Technical Report writing skills                         
  • Computer Systems Validation & GMP Guidelines
  • Interviewing skills
  • Opex mindset to drive and improve performance in QC

 

Upload your CV/resume or any other relevant file. Max. file size: 256 MB.