Job DescriptionControl, distribution, and administration of Quality documentation, which support Technopath's quality management systems.Process and approve document change requests followed by providing notification of changes to controlled documents to relevant parties.Maintenance of various logs associated with tracking of documentation or tasks.Incoming Quality Assurance: Maintain raw material specifications (file/update), complete check of raw material certificates of analysis, perform visual inspections.Perform batch record review.Support Technopath Internal Audit program.Performs other related duties as assigned by management.Demonstrate an understanding of the application of the Quality Policy through daily activities.
Maintain vigilance to ensure adherence to the policy and system procedures by promptly reporting noncompliance issues to management.QualificationsMinimum of degree qualification in a relevant Science, Engineering or QA subject area2+ years industry experience working in a regulated environment for medical devicesBasic knowledge of FDA 21CFR820, ISO13485, IVDD98/79/EC, IVDR EU/2017/746 and international regulatory requirementsExcellent communication skills and attention to detailAdditional InformationOUR VALUESPASSIONCURIOSITY INTEGRITYBRILLIANCERESPECT BenefitsJoin us and enjoy:25 days holidaysLife assurance & health allowanceDiscounts with local and national retailersFree 24/7 Employee Assistance ProgrammeRecognition schemes and monetary awardsAt 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