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Senior Technician Quality Control

Reference:RK26656
Location: Carlow
Qualification:Degree
Experience:2-3 Years
Job Type:Fixed Term Contract
Salary:Not Disclosed
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May be suitable for: QC Analyst

Senior Technician Quality Control
Onsite - Shift 2 cycle
RK26656
Contract 11 months
Carlow



We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



Key Responsibilities:

  • Ensure compliance with cGMP, GDP, data integrity (ALCOA) and regulatory requirements across all Quality activities.
  • Support the manufacturing, testing and release of vaccine and biologic products in accordance with site procedures and regulatory standards.
  • Collaborate with Quality, QC, Manufacturing and other departments to resolve quality-related queries and maintain compliance.
  • Identify and support continuous improvement and compliance initiatives to enhance operational efficiency.
  • Support business-critical projects within the Quality Department.
  • Perform laboratory testing, including analytical and microbiological testing, and material inspections to ensure specification conformance.
  • Maintain a safe, compliant and qualified laboratory environment, adhering to PPE and safety requirements.
  • Execute, review and support deviations, CAPAs, complaints, material qualification, validation and Quality Risk Management activities.
  • Review batch records, material documentation, SOPs, GMP data and other quality-related documentation.
  • Support the development, revision and implementation of SOPs, operational procedures and training materials.
  • Participate in training activities and provide support to team members as required.
  • Work shift patterns where required to support manufacturing and Quality operations.


Education and Experience:
  • Degree in Science, Engineering or similar
  • 2-4 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
  • Lean Six Sigma Yellow Belt or suitable alternative
  • Knowledge of cGMP in Laboratory Quality Systems.
  • Proficiency in Microsoft Office and job-related computer applications required


If interested in this posting, please feel free to contact Rachel Kent at Life Science Recruitment for further information.




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