Team Horizon is seeking a QC Analytical Analyst for our client in Sligo.Why you should apply:Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.You enjoy working on exciting projects and want to work with a global manufacturing site.What you will be doingEnsuring Analytical Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.Understanding Regulations and business processes required to maintain Laboratory Data Integrity.Ensuring timely completion of all laboratory analysis assigned to shift.Ensuring that analysts working in the assigned cell or team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance.Improving the overall efficiency and velocity within the assigned team.Identifying and implementing improvements in analytical practices using ‘Zero, Believe it, Achieve it’Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements.Identifying weaknesses in laboratory performance and working with the laboratory management to rectify.Supporting & initiating analytical OOS issues as they arise in a timely manner both through practical work and through the quality system.Ensuring 5S excellence is maintained across the Laboratory.Instilling a quality culture of Zero, Believe it, Achieve it amongst the laboratory teamEnsuring that all laboratory test equipment is utilised and maintained correctly.Maintaining up-to-date, complete and precise records of all tests performed.Investigates Documentation related events in production that have quality or compliance impact.Leads or participates IIA, RCI sessions.Documents investigation outcomes.Frequently interacts with functional peer groups. Interaction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects, schedules, etc.Comply with policies and procedures, Standards and Specifications, Plant procedures, and regulatory agencies regulations and requirements.What you need to applyBachelor’s Degree or equivalent preferential, preferably in a Science or related fieldExperience Level = 1+ YearsExperience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelinesProven track record in an analytical role.Proficient in using analytical equipment in a QC lab as well as troubleshooting.Knowledgeable in instrumentation such as UHPLC, SoloVPE, TOC, and Identification techniques.Experience in industry is essential.
#J-18808-Ljbffr