LSC, Life Science Consultants is seeking a Quality Assurance Senior Associate for a contract role in a South Dublin biopharmaceutical company. The ideal candidate will have over 4 years of experience in the pharmaceutical or biotechnology industry. Responsibilities include testing components, reviewing documentation, and training staff. Strong organizational, communication skills, and a problem-solving mindset are essential. Candidates must hold a Stamp 1G or Stamp 4 visa to apply. #J-18808-Ljbffr
Job Overview LSC has a great contract opportunity for a Quality Assurance Senior Associate to join a South Dublin based Biopharmaceutical company. If you have 4 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! Key Responsibilities Testing of primary and secondary components for use in the manufacture of aseptic products. Sampling of Excipients and Drug Substance under Grade C conditions. Review and approve documentation associated with component testing in preparation for QA Specialist or Qualified Person disposition activities. Compile, review and approve minor deviations and CAPAs for closure ensuring compliance with appropriate documentation, whilst ensuring that CAPA actions address root cause and implementation plan dates are achievable. Provide training and advice to staff in relation to testing of components and packaging. Actively participate in audits and their preparation. Review and approve cGMP records (e.g., WO, JP, GDMS, deviation, CAPA, protocols, reports, SOP, etc.) ensuring compliance with appropriate documentation. Education and Experience University degree in Engineering or Science related discipline. Relevant experience (4+ years) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role. Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Non-Conformance / Deviation investigations. Experience working in aseptic operations, protein formulation, vial and syringe filling. About You Strong organizational skills, including ability to follow assignments through to completion. Excellent written and verbal communication skills. Experience working with dynamic cross-functional teams and proven abilities in decision making. Must pass eye-tests required for visual inspection. Eligibility As this is a contract opportunity, you will need to hold a Stamp 1G/Stamp 4 visa to apply. #J-18808-Ljbffr
LSC, Life Science Consultants, is seeking a QA Validation Associate to join a Cork-based Biopharmaceutical company. The role involves providing quality oversight for validation activities, leading QA Validation discussions, and ensuring compliance with regulatory standards. Ideal candidates should have a Bachelor's degree in a relevant field and 3 years of experience in a cGMP environment. Applicants must have a Stamp 1G or 4 visa. Apply or contact Kathy Gillen at LSC for more information. #J-18808-Ljbffr
LSC has a great contract opportunity for a QC Instrument Engineer to join a Dublin-based biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life. If you have 3 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! About the Project – Key Responsibilities Providing a calibration and/or maintenance service to the QC laboratory that includes instrumentation calibrations, scheduling and tracking of instrument maintenance, and instrument lifecycle management. Review and approve analytical instrumentation qualification, calibration, repairs and documentation. Ensure instrument maintenance and verification is appropriate to the use of the instrument. Manage all instrument-specific investigations such as calibration deviations. Trend lab instrument performance and lifecycle management. Participate in new instrument purchase and qualification. About You – Are Your Skills a Match? The ideal candidate should hold a minimum of a B.Sc. in a scientific-related discipline and must have at least 3 years' experience, at least 1 of which should be related to instrument qualification experience in a GMP laboratory setting. Previous experience in technology transfers would be advantageous. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply. #J-18808-Ljbffr
LSC, Life Science Consultants, is offering a contract opportunity for a QC Instrument Engineer in Dublin. The successful candidate will provide calibration and maintenance services to a biopharmaceutical company's quality control laboratory. Key responsibilities include approving instrumentation qualifications and managing related investigations. Candidates should have at least 3 years of experience in the pharmaceutical industry and a B.Sc. in a scientific discipline. Holding a Stamp 1G/Stamp 4 visa is necessary for application. #J-18808-Ljbffr
Overview LSC have a great contract opportunity for a QA Validation Associate to join a Cork based Biopharmaceutical company. If you have 3+ years of experience within a GMP environment and are ready for your next challenge, this could be the perfect project for you! About the Project – Key Responsibilities Provide quality oversight for validation activities related to products and facilities, utilities, equipment (FUE). Support the development of validation plans for specific system implementation projects. Support validation activities related to the implementation of facilities, utilities, equipment changes, including the review/approval of project lifecycle documentation (URS, RA, Commissioning, Qualification Protocols), exercising judgement within broadly defined procedures to establish approval criteria and identify solutions. Support validation policies through development, generation and implementation of validation master plans, guideline documents and SOPs. Lead and represent QA Validation in multi-departmental meetings & project teams. Participation in the change control program for modifications to qualified systems. Quality oversight for the Revalidation Evaluation program. Identify, track and resolve issues through robust root cause analysis in a timely manner, working with relevant SMEs as required. About You – Are Your Skills a Match? Bachelor of Sciences degree, or higher, in a technical discipline (physical, engineering, chemical or biological sciences) is required. 3 years' experience in a cGMP regulated manufacturing environment, with knowledge of equipment and utility validation, and laboratory systems / validation. Organizational and management skills to coordinate multi-discipline project groups. Ability to speak, present data, and defend approaches in front of audiences and inspectors. Ability to comprehend technical information related to equipment, processes, and regulatory expectations. Experience with participation in regulatory inspections presenting or defending departmental functions in audits or regulatory inspections. Understanding and familiarity with FDA & European regulatory requirements, guidelines, and recommendations for equipment validation expectations. Applicants interested in contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please understand that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Kathy Gillen at LSC on 021-4777329 if you have any more questions about this opportunity! #J-18808-Ljbffr
LSC have a great contract opportunity for a Senior Quality Control Microbiology Associate to join a Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 2 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Environmental Monitoring of Grade 8/9 Cleanrooms. Environmental Monitoring of Grade 5/7 Cleanrooms & Isolators. Reading of Environmental Monitoring Plates. Bioburden testing of water & disinfectants. Writing technical reports. Testing of In Process samples such as Protein Concentration, Density & pH. ABOUT YOU - ARE YOUR SKILLS A MATCH? Experience working in an aseptic cleanroom performing Environmental Monitoring. Proficient in the use of LIMS & LMES. Technically strong background in microbiology and aseptic manufacturing. Flexibility – the EM role often encounters changing priorities on a daily basis. Refers to technical standards, principles, theories and precedents as needed. Biopharmaceutical QC experience in a microbiology lab. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Experience in LIMS, Change Control, Trackwise, SAP and CDOCS. Experience with Regulatory inspectors and interacting with inspectors desirable. Demonstrated ability to work independently and deliver right first time results. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! #J-18808-Ljbffr
Overview LSC have a great contract opportunity for Microbiologist to join a leading Cork based pharmaceutical company. As a Sr Scientist - Microbiology in the TSMS team you will provide technical and operational support across process microbiology and environmental/utility microbiology activities across the site. The role is focused on execution of routine and planned microbiology activities, data generation and analysis, quality and compliance support, and preparation of technical documentation. What you will do: Execute routine TSMS microbiology activities in support of manufacturing operations, including process microbiology and EM/Utilities microbiology. Support Environmental Monitoring (EM) and utilities microbiology programmes through data review, trending, and issue follow up. Provide day-to-day microbiology support to operations, laboratories, engineering, and quality functions as required. Support deviation investigations, root cause analysis, and CAPA development related to microbiological events. Ensure activities are performed in compliance with GMP, site procedures, and regulatory expectations. What We're Looking For: Bachelor's degree (or higher) in Microbiology, Biological Sciences, or a related discipline. 4+ years experience working as a microbiologist in a GMP regulated pharmaceutical or biotech environment. Demonstrated hands on experience in Process microbiology, Environmental Monitoring (EM), and Utilities microbiology (e.g. water systems, clean steam). Data systems and compliance systems appropriate to the role. Apply via this advert or contact Kathy Gillen at +353 214718212 if you have any more questions about this opportunity. As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply. LSC do not provide work permit sponsorship. #J-18808-Ljbffr
LSC have a great contract opportunity for QA Associate SAP to join a leading Cork based pharmaceutical company. SAP Quality & Operations Specialist – Cork, Ireland Join a dynamic team supporting SAP Quality and operational excellence in Cork. This role is ideal for someone with SAP experience in a GMP/GDP environment, looking to collaborate across global supply chain, quality, and manufacturing teams. What You'll Do Support and troubleshoot SAP QM processes and data, including Material Master, inspection plans, and batch records. Train end users and act as the main interface with global SAP and business teams. Execute overrides, manage inspection lots, and maintain quality-critical data. Contribute to daily Quality Management System activities: supplier/customer qualification, risk assessments, change controls, audits, and documentation. Perform contract manufacturing stock reconciliation and support annual counts. What We're Looking For Honours Bachelor's in Supply Chain or a scientific discipline. 3+ years SAP experience in a GMP/GDP environment. Strong analytical, problem‑solving, and relationship‑building skills. Ability to work independently and as part of a team. Why Join Us Collaborate with global teams in a high‑impact environment. Work on SAP QM processes critical to operational excellence. Opportunities for continuous improvement and professional growth. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! Apply via this advert or contact Siobhan Cummins at +353 214 771 329 if you have any more questions about this opportunity. #J-18808-Ljbffr
LSC, Life Science Consultants is seeking a QA Associate SAP to join a leading pharmaceutical company in Cork, Ireland. This role supports SAP Quality Management processes and requires 3+ years of SAP experience in a GMP/GDP environment. Responsibilities include troubleshooting SAP data, training end users, and contributing to quality management activities. Opportunity for continuous improvement and professional growth within a dynamic team environment. Eligible candidates must hold a Stamp 1G/4 visa to apply. #J-18808-Ljbffr
