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Teva Facilitator QC Team Lead 
Ireland 
771183352

25.06.2024

Key Responsibilities:

  • 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
Working Hours

This role is based on a 2 shift cycle - Day shift 6am – 2pm & Evening shift 2pm – 10pm

Are you?

  • Degree level educated within a scientific discipline

Do you have?

  • Knowledge of cGMP, and GMP for Labs requirements.

  • Broad Knowledge of Analytical Techniques and Experience in HPLC/UPLC

  • 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

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Internal Eligibility for Job Postings

Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:

  • Be a current employee of Teva

  • Meet the basic requirements for the job

  • Have received a rating not lower than “Successful” on their most recent performance review and must not currently be on a performance improvement plan

  • Apply to the posted requisition within the allotted time frame

  • Have been in their current position for a minimum tenure of twelve (12) months

Unless explicitly stated in the job description, no company sponsored work authorisation no relocation assistance should be assumed.