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Manufacturing Quality Assurance Specialist

LGC Group


Job Location:

Tipperary - Ireland

Monthly Salary: Not provided by the employer
Posted: 7 July 2026 (30+ days ago)
Application Deadline: 4 October 2026
Vacancies: 1 Vacancy

Job Summary

Join LGC as a Manufacturing Quality Assurance Specialist in the scenic town of Tipperary Ireland. Become part of a highly motivated team committed to delivering perfect quality in all we do. If you have a passion for quality assurance and want to work alongside top professionals this role is for you!

Job Responsibilities

  • Perform batch record review to release raw materials components and finished devices.
  • Review and approve protocols reports and documentation updates ensuring adherence to Technopath Clinical Diagnostics (TCD) procedures/policies and regulatory requirements.
  • Ensure accurate use of statistical QA methods in the production environment.
  • Apply quality tools to monitor and analyze quality performance. Identify important opportunities for improvement. Ensure all process developments follow the Quality Management System.
  • Implement quality systems and detailed approaches across Technopath Manufacturing businesses.
  • Ensure adherence to all detailed Quality Management System requirements as per ISO13485 MDSAP IVDD IVDR and FDA.
  • Conduct internal audits as needed to verify that TCDs quality management system meets the requirements of ISO13485 MDSAP IVDD IVDR and FDA.
  • Offer training on processes as needed to ensure adherence to the quality management system.
  • Ensure adherence to internal procedures and regulatory requirements for the secure handling storage documentation and accountability of controlled drugs as applicable to the role.
  • Maintain a high level of housekeeping in designated areas and observe all Health and Safety at work requirements.
  • Provide assistance to other departments within Manufacturing Quality Assurance when required

Qualifications :

  • . in Science Engineering QA or a related field or equivalent experience.
  • A minimum of 3 years of practical experience in a quality function.
  • Knowledge of FDA 21CFR820 ISO13485:2016 IVDD98/79/EC IVDR/EU/2017/746 and international regulatory requirements.
  • Excellent communication skills and attention to detail.
  • Ability to work on own initiative and within a team.
  • Strong troubleshooting skills.

Be part of a team where your contributions make a significant impact and work in a role that offers both challenge and reward. Here at LGC we value collaboration proven expertise and the drive to compete on a global scale. Successfully implement your skills and determine the future of quality assurance with us!


Additional Information :

Our values

  • PASSION
  • CURIOSITY
  • INTEGRITY
  • BRILLIANCE
  • RESPECT

Benefits

Join us and enjoy:

  • 25 days holidays
  • Life assurance & health allowance
  • Discounts with local and national retailers
  • Free 24/7 Employee Assistance Programme
  • Recognition schemes and monetary awards

At LGC we foster a culture of inclusion and collaboration. We believe that diverse perspectives lead to better outcomes and encourage applicants from all backgrounds to apply. We are an equal opportunity employer and offer reasonable accommodations to individuals with disabilities. If you require any adjustments throughout the recruitment process please let us know.

Join us in this outstanding opportunity to be part of a company that is leading advancements in the industry!

#lgcij


Remote Work :

No


Employment Type :

Full-time


About Company

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With over 180 years of scientific heritage and operations in 14 countries, our products and services are integral to the industries that safeguard our food, water, medicine, and environment. Working collaboratively with our partners across the scientific community, our solutions addr ... View more

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