Job InformationDate Opened11/19/2025Job TypeFull timeIndustryPharma/Biotech/Clinical ResearchWork Experience1-3 yearsCityCarlowState/ProvinceCarlowCountryIrelandJob DescriptionAbout PSC BiotechWho are we?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.'Take your Career to a new Level'PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.Employee Value PropositionEmployees are the "heartbeat" of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client's expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.Overview:As QC Analyst you will perform and review a range of techniques such as immunoassays, cell based potency bioassays HPLC and compendial methods as part of routine and non-routine testing and project work to ensure processes and end products comply with corporate and regulatory requirements to facilitate product release. Reporting to the QC Manager you will ensure that objectives are effectively achieved, consistent with our requirements to ensure compliance, safety and reliable supply to our customers.Our QC group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.Shift Pattern 2-cycle: 7am to 3pm week 1; 2:30pm to 10:30pm week 2RequirementsResponsibilities:Work as directed by the QC Manager / Associate Director, according to Company safety policies, cGMP and cGLP.Required to drive compliance with our Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.Required to comply with our Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.Develop, implement and maintain procedures that comply with appropriate regulatory requirements.Ensure that all Quality Systems within the department are adhered to on a daily basis.Operate as part of the QC team performing the allocated testing and laboratory-based duties.Ensure timely completion of all assigned data processing and reviewing.Ensure timely completion of Laboratory Investigation Reports and deviations through site proceduresParticipate in the timely generation of trend data, investigations, nonconformances, validation protocols, reports in support of method validation/verifications and equipment qualifications.Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc.Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.Where applicable, review, approve and trend test results.Participate in the laboratory aspects of OOS investigations.Provide support with audit/inspection requirements to ensure department compliance/readiness.Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility.Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g. FMEA, Fishbone diagrams, 5 why's etc,Work collaboratively to drive a safe and compliant culture.May be required to perform other duties as assigned.Reporting Structure: Reports to QC ManagerQualifications:TechnicalKnowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.Knowledge of cGMPLaboratory Quality SystemsProficiency in Microsoft Office and job-related computer applications requiredReport, standards, policy writing skills requiredUnderstanding of Lean Six Sigma Methodology preferred.Immunoassay and cell culture experience preferablePeopleA great communicator, decisive decision-maker with a proven ability to deliver excellenceAbility to participate in highly-effective teams.The desire to continuously learn, improve and develop.Strong leadership and interpersonal skills.Willingness to support the team and a strong focus on delivering excellence.High personal integrity, credibility, energy and flexibility.Model the leadership behaviours and use the MPS principles to achieve success.Set clear performance standards; overcome obstacles; hold ourselves and others accountable for achieving results.Education:Bachelor's Degree or higher preferred; ideally in a science related discipline.