QC Analyst at LGC Group

Ballina, Munster, Ireland -

Full Time

Start Date

Immediate

Expiry Date

29 Mar, 26

Salary

0.0

Posted On

29 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Testing, Equipment Maintenance, Technical Investigations, GLP Standards, GDP Standards, Problem Solving, Attention to Detail, Teamwork, Communication Skills, Microsoft Office Proficiency

Industry

Biotechnology Research

Description

Company Description LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of catalogue and custom-developed diagnostic quality solutions and component materials for the extended life sciences industry. We partner with IVD assay developers, and pharmaceutical, CRO and academic institutions in commercialization activities across the entire diagnostic pipeline. Laboratorians and diagnostic professionals across disciplines of clinical chemistry, immunochemistry, serology, molecular diagnostics, and clinical genomics rely on LGC’s products to support accurate and reliable diagnostic results. Our operating entities include Maine Standards Company, SeraCare Life Sciences, and Technopath Clinical Diagnostics, which are in vitro diagnostics (IVD) manufacturers of quality measurement tools (calibrators, controls, linearity, EQA/PT, biological materials), the Native Antigen Company, which is a manufacturer and supplier of viral antigens and LGC Proficiency Testing a global leader in PT schemes. We operate FDA-registered and ISO 13485-accredited facilities in Maine (USA), Massachusetts (USA), Maryland (USA), Tipperary (Ireland), ISO 9001-accredited facility in Oxford, UK, and Traverse City, Michigan US. Each day, our world-class staff, scientific expertise, operational efficiency, and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes - from the widely adopted and established through to cutting-edge NGS and precision diagnostics. Job Description Are you ready to begin your career in a scientific environment? As a QC Analyst, you will play a vital role in ensuring the integrity of our products while gaining hands-on experience with clinical laboratory instruments. This is a fantastic opportunity to grow within a world-class QC team and contribute to our commitment to excellence. In this role, you will develop proficiency in analytical testing, support equipment maintenance, and assist with technical investigations. You will work collaboratively to detail QC data, lead inventory, and uphold rigorous GLP and GDP standards. Job Purpose QC analysts must develop testing proficiency across clinical laboratory instruments and become proficient in completing QC release analysis, value assignment, and any testing to outstanding GLP (Good Laboratory Practice) standards. Teamwork, ability to multitask, problem solving and attention to detail are key skills for this role. Key Responsibilities Become proficient in performing analysis using various clinical laboratory instruments. Complete routine maintenance and troubleshoot issues on all laboratory equipment. Perform value assignment and target value testing for Technopath products. Perform QC release analysis for Technopath products including, stability testing, bioburden analysis, physical appearance inspections. Assist in technical investigations and other testing requests as required. Work with the QC team to analyse, collate and document QC generated data within specified timelines. Ensure outstanding GLP and GDP standards are maintained. Responsibility to lead QC inventory, including stock monitoring. preparation of material orders and other tasks as assigned. Identify and communicate areas for continuous improvement. Performs other related duties as assigned by QC Manager. Qualifications BSc qualification or equivalent experience in a relevant Science field is preferred. Preferable minimum 3 years’ experience in a laboratory or other regulated medical product environment. Proficiency on Microsoft office is required. Knowledge of GLP and GDP requirements. Excellent attention to detail, problem solving skills and ability to prioritise workload. Positive attitude, flexibility, and ability to work in a team driven environment. Strong interpersonal and communication skills both verbal and written. Additional Information ABOUT LGC: LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range. OUR VALUES PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT EQUAL OPPORTUNITIES LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website www.lgcgroup.com #scienceforasaferworld #LGCIJ Work Arrangement: On-site Department: Scientific / Technical Science

Responsibilities

QC Analysts will perform analysis using clinical laboratory instruments and complete routine maintenance on laboratory equipment. They will also assist in technical investigations and ensure compliance with GLP and GDP standards.