LSC has a great contract opportunity for a QC Senior Analyst to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra‑rare disorders through the innovation, development and commercialization of life‑transforming therapeutic products. If you have 4 years of experience working in the biochemistry, pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! Key Responsibilities Perform all lab functions in compliance with cGMP. Follow written procedures for the following tests, as trained and qualified: Gel electrophoresis (SDS‑PAGE, IEF). ELISA and plate‑based assays (potency and residual assays such as HCP and ProA). Stability scheduling and testing. Recognize and report aberrant test results and sample conditions. Provide QC SME and day‑to‑day technical guidance to QC biochemistry analysts. Lead and complete the execution of investigations/CAPAs in a timely manner. Provide lab support including reagent preparation, cleaning, and routine equipment maintenance. About You BSc in Chemistry or a biological science. 4–7 years of experience with gel electrophoresis (SDS‑PAGE, IEF), ELISA and plate‑based assays. A working knowledge of the cGMP QC laboratory environment, and the equipment associated with testing of biopharmaceutical products. 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 Kathy Gillen at LSC on 021 4781212 if you have any more questions about this role. #J-18808-Ljbffr
LSC, Life Science Consultants is seeking a QC Senior Analyst for a biopharmaceutical company in Dublin. The role requires performing lab functions in compliance with cGMP standards, engaging in gel electrophoresis and ELISA testing, and providing technical guidance to QC analysts. Candidates should possess a BSc in Chemistry or biological science and have 4-7 years of experience in the biochemistry or biotechnology industry. This contract opportunity requires eligibility to work in Ireland with necessary visa documentation. #J-18808-Ljbffr
LSC have a great contract opportunity for a Research Associate to join a Cork based Biopharmaceutical company. If you have 1+ 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 Executes defined procedures independently to support studies and investigation activities with lab scale upstream processes in the multi-product lab. In addition to quick learning of core scientific techniques, principles and protocols, owns small project portions reliable execution and able to summarizes findings. Understanding the principles of aseptic operation and experience in working in biosafety cabinets. Daily operations with microbial cell culture (E. coli), including cell thawing and cell banking, seed train expansion etc. Experience in fermentation process, including fermenter inoculation, daily monitoring, sampling and in-process analysis utilizing standard bioprocess analytical equipment. Basic understanding of mammalian cell expansion and it's difference in comparison to microbial operations. Expands technical toolkit by adapting and troubleshooting process steps or assays, applies appropriate methods and interprets basic data trends. ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's degree or higher in Science or Engineering. A minimum of 1 year experience in the pharmaceutical industry or equivalent strong laboratory experience. Working knowledge of pharmaceutical regulatory requirements appropriate to level and understanding of the cGMP manufacturing process for Biologics. Understanding of fed-batch and perfusion bioprocesses. Experience in depth filtration and ultrafiltration. Understanding of downstream purification process. Applicants interested in our 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. #J-18808-Ljbffr
LSC, Life Science Consultants is hiring a QC Analyst for a biopharmaceutical company in Athlone. The role involves supporting Chemistry and Microbiological testing, ensuring compliance with cGMP and GLP standards, and performing technical reviews. Candidates should have a BSc (Hons) in biosciences and 3 years of experience in a QC lab. Strong analytical and technical writing skills are necessary. The position is contract-based and requires eligibility to work in Ireland. #J-18808-Ljbffr
LSC, Life Science Consultants, is offering a contract opportunity for a Research Associate in Cork, Ireland. The ideal candidate will possess a Bachelor's degree in Science or Engineering and have at least 1 year of experience in a GMP environment. Responsibilities include executing procedures for upstream processes, conducting microbial cell culture, and understanding bioprocesses. Applicants must have the right to work in Ireland with a Stamp 1G or 4 visa. No visa sponsorship is available. #J-18808-Ljbffr
LSC, Life Science Consultants is offering a contract opportunity for a QC Chemistry Senior Analyst in Dublin. The successful candidate will be responsible for conducting lab functions in compliance with cGMP and will support training of new analysts. A BSc in Chemistry or a biological science and over 3 years of experience in HPLC analysis within a GLP lab setting are required. This position is crucial for a biopharmaceutical company focused on innovative therapies. #J-18808-Ljbffr
LSC have a great contract opportunity for a QC Chemistry Senior Analyst to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products. 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: Perform all lab functions in compliance with cGMP. Follow written procedures for the following tests, as trained and qualified. Stability scheduling and testing. Recognize and report aberrant test results and sample conditions. Provide QC SME and day to day technical guidance to QC Chemistry analysts. Training of new analysts in specific assays. Drive continuous improvement initiatives within the QC department. Lead and complete execution of investigations/CAPAs in a timely manner. Provide lab support including reagent preparation, cleaning, and routine equipment maintenance. ABOUT YOU - ARE YOUR SKILLS A MATCH? BSc in Chemistry or a biological science. 3 + years' experience with HPLC analysis in a GLP laboratory setting. 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 Jenny Murphy at LSC on 021 4777329 if you have any more questions about this role! #J-18808-Ljbffr
Key Responsibilities The DRY External Manufacturing Quality Assurance Contractor provides support to all quality activities at Contract Manufacturing organizations (CMs). The QA Contractor’s position is essential for ensuring that all batches meet specifications, are manufactured in accordance with the validated process and are compliant to cGMPs and regulatory commitments. Escalate quality issues at CMs to QA management. Assist in the establishment and revisions of Quality Agreements with affiliates and customers. Ensure compliance with Quality Agreements and Manufacturing Responsibilities Documents (MRDs). Coordinate and perform QA responsibilities of API shipments. Participate in regulatory inspection preparations with CMs and provide on-site support during inspections. Participate on the Technical Review Board. Evaluate and disposition API batches, if required. Ensure that documented checks have been completed for the Certificates of Testing and Certificates of Environmental Monitoring (where applicable), and deviations, changes and batch documentation that demonstrates requirements have been met prior to batch release. Provide quality support of API manufacturing with the focus on holistic review of key activities associated with or impacting the manufacturing processes including deviations, change controls and countermeasures. Ensure all processes are in an appropriate state of control. Participate in APR activities. Participate in Joint Process (JPT) and Post Launch Optimization (PLOT) Teams. Basic Requirements BS in a science‑related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences. Previous GMP manufacturing knowledge and/or experience in API or finished product manufacturing, QC, QA or Engineering. Additional Preferences Experience in quality support for Quality Control activities. Knowledge of pharmaceutical manufacturing operations. Demonstrated coaching and mentoring skills. Experience in root cause analysis. Demonstrated application of statistical skills. Demonstrated strong written and verbal communication skills. Strong attention to detail. Proficiency with computer system applications. Education Requirements BS in a science‑related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences. Visa and Eligibility Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a valid Stamp 1G/Stamp 4 visa to apply. #J-18808-Ljbffr
LSC, Life Science Consultants is seeking an Associate Scientist in Dublin. Join a biopharmaceutical company dedicated to innovative medicines and contribute by providing technical support for analytical methods. Candidates should have 3+ years in the pharmaceutical or biotech industry, and a PhD, MSc, or BSc in relevant fields. Solid experience in analytical methods and a strong understanding of biological products is essential. This position does not offer visa sponsorship. #J-18808-Ljbffr
LSC, Life Science Consultants is looking for a Senior Cleaning Validation Lead to join a biopharmaceutical company in Dublin. This role involves providing cleaning expertise across various equipment, authoring crucial documentation, leading a team of specialists, and ensuring compliance with cGMP requirements. Candidates should have over 10 years of experience in pharmaceuticals or biotechnology, with a strong background in Cleaning Validation and a relevant undergraduate degree. A Stamp 1G/Stamp 4 visa is required for eligibility. #J-18808-Ljbffr
