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Lgcgroup

Lgcgroup

Manufacturing Quality Assurance Specialist

Company

Lgcgroup

Role

Manufacturing Quality Assurance Specialist

Location

Tipperary, IRELAND, ie

Job type

Full-time

Found on Mokaru

Yesterday

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Salary

Not disclosed by employer

Job description

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 TCD’s 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
  • B.Sc. 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!

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!

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