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Laboratory Analyst – Glasgow (Job Ref: 26/LBGS) Randox are a world leader in diagnostics for clinical healthcare, toxicology, and food security. Our expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Our global success is a result of our pioneering products, the commitment and skill of our workforce, which continues to grow. We are currently looking to hire Laboratory Analysts within our team based in Glasgow. The successful candidate will be conducting rapid onsite testing for multiple Point of Care clinical and / or molecular tests. The role will be responsible for the processing of blood and other samples from Randox Health or third-party clinics. Location : 150 Howard St, Glasgow, G1 4ET. Contract Offered : Full-time, permanent. Working Hours / Shifts : 4 on, 4 off: either 7am to 7pm or 9am to 9pm. For this position, as you may be in contact with live blood samples, you must be vaccinated against Hepatitis B or be able to get it following a successful interview stage. Right to Work Requirement Please note that this role requires candidates to have the legal right to work in the UK for a minimum of 12 months from the application date. This is to ensure completion of our 9-month probationary period and for any potential sponsorship decisions to be considered. Unfortunately, we are unable to offer visa sponsorship at the point of hire. What does this role involve? This role is responsible for routine clinical testing in our laboratory. The main duties of the role include: • Routine use of the Laboratory Information Management System (LIMs). • The performance of various analytical procedures including various manual screening and automated methods covering a wide variety of clinical diagnostic tests. • The preparation and handling of samples and diagnostic reagents. • The operation of various automated analytical systems such as the Bosch Vivalytic. • Strict adherence to chain of custody procedures throughout the analytical process. • The routine maintenance and calibration of analytical instrumentation. • The preparation of specimens for transportation to ensure that their stability is safeguarded during shipment to the appropriate analytical laboratory. • Recording and Monitoring of temperature for Laboratory and Equipment. • Perform troubleshooting on technical issues associated with Clinical Diagnostic Testing. • Ensuring that all the necessary Quality Control checks are completed daily and that they meet internal criteria. • Participation in Quality Audits. Essential: • Qualified to at least degree level in Biochemistry or a life science. • Demonstrable experience of working with strong attention to detail. • Excellent analytical and problem-solving skills. • Excellent communication and organisational skills. • Currently have the right to work in the UK without visa sponsorship. Desirable: • Practical experience using automated analysers. • 1 year laboratory-based experience as Scientist or a Lab Analyst. • Experience in a private healthcare setting. • Working knowledge of quality systems • Working knowledge of Health and Safety, including CoSHH. • Flexibility to work overtime when needed.
DAM Business Analyst
DAM Business Analyst Glanbia Enterprise Solutions Role Overview The DAM (Digital Asset Management) Business Analyst acts as a key bridge between the Business and IT by translating Business needs into detailed requirements and technology-enabled use cases. They develop a deep understanding of the opportunities, risks, and issues facing the Business, and advise on how technology solutions can be used to achieve / resolve them. This permanent opportunity reports to the Foundation Tech Product Manager. Key Responsibilities Strategic Alignment & Business Engagement Where and how you will work The opportunity will be based in Citywest, Dublin 24 with hybrid working arrangements available which offer you a greater choice in how you work and live, giving you a better work-life balance. What we would like to offer you! The opportunity to develop your career on a global stage, continuous learning through an on-demand learning platform, and a competitive compensation package including staff discounts, generous family leave policy, competitive salary. About Glanbia Glanbia is a better nutrition company with three divisions: Performance Nutrition, Health & Nutrition and Dairy Nutrition. Collectively and with our partners we offer an incredible breadth of expertise in nutrition. We employ a team of 5800 people, work with global food and beverage companies, and sell our award-winning and market-leading brands and ingredients in more than 100 countries worldwide At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a variety of candidates, we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia, our culture celebrates individuality, knowing that together we are more.
Data and Document Reviewer
OVERALL ROLE OBJECTIVE: Team: Analytical Services To be responsible for the checking and reviewing of analytical data and documents (SOPs, protocols, reports etc) To develop and implement efficient manual/electronic systems and procedures for the storage, searching, trending and retrieval of analytical data and documents. JOB SPECIFIC RESPONSIBILITIES: The post holder will: 1. Prepare and review analytical documentation, such as protocols, reports, SOPs and AOIs. 2. Check and review analytical data to ensure compliance with internal SOPs and if relevant specific customer requirements. 3. Compile and deliver training packages in accurate, timely and right-first-time documentation. 4. Critically assess and propose improvements to working practices with respect to analytical data packages, document templates and electronic systems for the storage and retrieval of analytical data and documents. 5. Generate, monitor and facilitate the improvement of relevant KPIs e.g. % right first time documentation. 6. Keep their supervisor informed on a regular basis of progress and any circumstances that alter agreed timescales. 7. Ensure that good housekeeping standards are maintained at all times. 8. Retain an up to date knowledge of analytical techniques and equipment. 9. Perform other duties as may be deemed appropriate by their supervisor and that fall within the general remit of the post. 10. Ensure that unplanned deviations (UPDs) are kept to a minimum and that your line manager is notified as soon as UPDs are generated. 11. Ensure that any corrective or preventative action arising from UPDS is completed in full and within allocated timeframes. 12. Assist with the identification of alternative test methods and/or equipment to improve efficiency and maximise throughput of testing in the laboratories. 13. Make suggestions for the improvement of efficiency and/or reduction in operating costs within the Quality Unit and the wider company. QUALIFICATIONS GCSE (or equivalent) passes, grades A-C, in Mathematics and English Language Degree level qualification (or equivalent) in an Analytical related discipline EXPERIENCE Previous experience in the preparation and review of analytical protocols, reports and data in a GMP/GLP environment. Previous practical experience of a wide range of analytical techniques and associated commercial data capture systems. KEY SKILLS Excellent communication skills (verbal and written) Quality focused and driven Excellent organisational skills Proven ability to work effectively on own initiative and effectively contribute within a team environment Proficient in the use of Microsoft Packages (Word, Excel, PowerPoint etc)
