Project Manufacturing Engineer (BBBH28170) Cork, Republic of Ireland LSC have a great contract opportunity for a Manufacturing Project Engineer to join a leading medical device company in Cork. If you have a 3 years’ experience as a manufacturing engineer in the medical device industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Leading and supporting various cost saving and time improvement projects Providing technical leadership on all product and process issues Line performance monitoring and the compilation and execution of structured event plans to remediate systemic issues that drive sub-optimal performance Development and implementation of appropriate supporting documentation, and process work instructions compliant with current Good Manufacturing Practices (GMP) Leading technical improvement under the team’s Continuous Improvement Program (CIP) ABOUT YOU - ARE YOUR SKILLS A MATCH? 3+ years’ experience in Medical Device as manufacturing or project engineer implementing change control in manufacturing NPI/Tech transfer experience and experience with EU-MDR regulations desirable. 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! To apply, submit your CV via this advert or contact Cian Marnane at LSC on 021-4777239 if you have any more questions about this Project Engineer opportunity! #J-18808-Ljbffr
LSC has an exciting opportunity for a HVAC Design Engineer to join a pharmaceutical company in Cork. This will be a dynamic environment that is constantly innovating, relies on cutting-edge technology to deliver life-saving medicines. You will be working in a site that supplies active ingredients through complex chemical synthesis and biotechnology manufacturing processes for a range of therapeutics. This is a chance for you to work with a global company that strives for excellence in every aspect of its operation and has a huge reputation for its diverse working culture. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Responsible for the HVAC and Fire Protection Design as part of a multi-discipline projects team. Generating detailed scope of work packages for HVAC contractor for tender/procurement process. Co-ordination and supervision of HVAC contractor(s) during construction and commissioning activities. Co-ordinate contractor activities to monitor and track work ensuring delivery of the schedule and budget. The Specification and procurement of AHU's etc. Preparation of HVAC Deliverables, including Project Management and control of HVAC Projects including cost estimates and reporting. ABOUT YOU - ARE YOUR SKILLS A MATCH? A BE degree in Engineering is preferred along with 5+ years' experience in HVAC Design/Construction environments. Candidate must have proficiency in a windows-based environment and software (Word, PowerPoint, Project, advanced Excel, and Access). 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! Call Stephen Abdullah at LSC on 021 4777 329 to discuss this new role in detail or apply directly via this advert. #J-18808-Ljbffr
LSC have a great contract opportunity for a Senior Process Engineer to join a global Biopharmaceutical company in Cork. The facility specializes in the fermentation, purification, and sterile filling of biotech products, as well as supporting product development and clinical trials. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Provide process engineering services in support of the design and commissioning & qualification of a significant expansion to an existing bulk vaccine processing facility. The job-holder works with the Process Engineering Team as a client owner representative to deliver Project Objectives. The Senior Process Engineer will manage cross functional teams to deliver the following scope; Equipment package design, factory acceptance testing, installation and commissioning Packages may include Product Vessels, Single Use Mixers, Single Use UFDF skids & CIP/SIP skids. Support Process Lead to implement a Process Design based on the scope of Process Requirements outlined in the project scope of work. Lead cross-functional project teams to ensure project and site stakeholder inputs and requirements are clear and reflected in C&Q deliverables. Liaise with stakeholders, equipment vendors, business partners, and SMEs at other sites within the Manufacturing Network as required to support Project. ABOUT YOU - ARE YOUR SKILLS A MATCH? Minimum qualification B.Sc. or M.Sc./ M.Eng Degree in Chemical or Biochemical Engineering or equivalent discipline; equivalent is defined as a Biotechnology or Industrial Chemistry Degree with basic the elements of chemical/biochemical engineering fundamentals as applied to biotechnology/bioprocessing. Minimum of 6 years post academic process engineering experience in relevant biopharmaceutical processing design, construction & start-up environment. In depth understanding of process engineering and technologies pertinent to unit process and utility operations for a bulk vaccine/biologics processing facility. 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 Adam Murphy at +353 21 4777329 if you have any more questions about this opportunity! #J-18808-Ljbffr
Automation Infrastructure Lead (BBBH28107) Cork, Republic of Ireland LSC have a great opportunity for an Automation Infrastructure Lead to join a market leading global Automation systems OEM with an extensive product (HW & SW) and service offering. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Support and administer DeltaV systems, ensuring smooth operation. Maintain DeltaV infrastructure, including servers, security tools, and applications. Lead automation hardware/software upgrades and new technology implementation. Monitor system health and resolve hardware issues. Configure and test platform equipment (servers, switches, workstations, thin clients). Coordinate infrastructure upgrades and system changes, updating documentation. Troubleshoot, identify root causes, and provide technical support. ABOUT YOU - ARE YOUR SKILLS A MATCH? 5+ years in automation, preferably in Pharma. Strong problem-solving, planning, and organizational skills. Self-motivated, able to work independently and in teams. Excellent communication and collaboration abilities. Knowledge of GMP, regulatory requirements, and system validation. PREFERRED: DeltaV training and experience with industrial networks/protocols (OPC, Ethernet IP). Virtualization technologies (Vertex, HCI), thin clients, and electronic testing (e.g., Kneat). 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 Paul O Driscoll at +353 214771329 if you have any more questions about this opportunity! #J-18808-Ljbffr
QA Operations Specialist (BBBH28233) Dublin, Republic of Ireland LSC have a great contract opportunity for QA Operations Specialist to join a leading biotech company based in Dublin. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures Provides presence on the shop floor to support compliance and data integrity QA support, review and approval of Commissioning and Qualification lifecycle documents for capital projects and new equipment. Will serve as the Quality SME for Performance qualification (PQ) activities across the site including but not limited to: Equipment, Facility and Utility PQ studies, Cleaning Validation, SIP, process validation Participates as the quality member on cross functional projects Support sustaining activities such as Change Management, Deviations, CAPAs, Equipment Requalification and Periodic review, Site Maintenance & Calibration Program ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor degree, in a scientific or engineering field (preferred) Minimum 5 years of relevant post-degree work experience in GMP Manufacturing, Quality Assurance or Laboratory environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing or laboratory operations. Evidence of leadership skills coupled with good oral and written communication skills Quality systems, pharmaceutical manufacturing or laboratory processes, authoring and approving GMP documents Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available currently. Apply via this advert or contact Grainne Hodnett on 021 4777 329 if you have any more questions about this opportunity! #J-18808-Ljbffr
LSC have a great contract opportunity for a QC Chemist to join a market leading, top Ten Biopharmaceutical company based in Cork. If you have 2+ years experience in a GMP regulated environment, with exhibited knowledge or proficiency in a compliance or quality role and are ready for your next challenge, this could be the perfect project for you! The Position QC Chemist in QC Commercial group supporting Bioanalytical/analytical testing supporting testing plans across multiple products. This is a pivotal role in terms of execution and delivery for the business and supporting test and release of priority lots. The role supports activities related to structured problem solving, technical support for laboratory investigations and support teams such as safety, 5S, Good lab practices and training. Job duties include: Coordinates waste management, LEAN/Operational excellence and 5S efforts as required. Supports testing of finished product across a variety of techniques for the solid oral dosage, sterile and biologic product portfolio. Troubleshoots standard instrumentation/test methods. Writes and revises methods, specifications, and SOP's as needed. Knowledge, Experience and Skills: Chromatographic separations experience in UPLC/HPLC and Empower. Working knowledge of GMPs, GLPs, pharmacopoeial, and regulatory requirements for testing and validation pertaining to the pharmaceutical industry is required. The ability to analyse data with a logical approach to problem solving and troubleshooting. Education & Experience: BSc degree in analytical Biochemistry or equivalent. Prior experience in pharmaceutical industry is preferred. 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 Kieran Mc Carthy at LSC on 021-4777329 if you have anymore questions about this QC Chemist - II opportunity! #J-18808-Ljbffr
CAD Engineer (BBBH28232) Cork, Republic of Ireland LSC have a great contract opportunity for a CAD Engineer to join a Pharmaceutical company in Cork. ABOUT THE PROJECT – KEY RESPONSIBILITIES Track, manage and store engineering drawings as per site procedures. Preparation of Process, electrical / instrument & layout drawings from rough sketches & oral instructions. Update Process, electrical / instrument & layout drawings from hand over packs for red line corrections. Issuing tags for all plant equipment & instruments installed by or for the engineering department. Ensuring all Engineering Consultants use the relevant Drafting, Drawing Labelling and Tags. Contribute to ongoing development of the department systems and procedures. ABOUT YOU - ARE YOUR SKILLS A MATCH? 4+ years of experience within a GMP environment. A bachelor's degree in relevant engineering or science degree. 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 Stephen Abdullah at LSC on 021-4777329 if you have any more questions about this opportunity! #J-18808-Ljbffr
Operations Lead (BBBH28229) Dublin, Republic of Ireland LSC have a great contract opportunity for an Operations Lead to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. ABOUT THE PROJECT – KEY RESPONSIBILITIES: Function as the site interface between the Product Delivery Teams (PDT’s), and Manufacturing operations. Develop, review, and approve Generic Master Batch Records and Parameter Value Lists across Formulation, Filling and Inspection. Develop, review and update Production, Engineering, Operating Procedures & training materials. Documentation and approval of protocol deviations for manufacturing activities. Consult with Process Development, Direct manufacturing, Equipment, and System Owners regarding process changes in an effective and timely manner. Own and lead change controls as required by the Manufacturing support team. ABOUT YOU – ARE YOUR SKILLS A MATCH? Bachelor’s degree in a science discipline. 3+ years of biopharmaceutical manufacturing experience in Fill Finish or related manufacturing or GMP experience in the pharmaceutical or medical device industry. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical 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 Adam Murphy on 021 4777329 if you have anymore questions about this role! #J-18808-Ljbffr
Process Development Sr Scientist (BBBH28224) Dublin, Republic of Ireland LSC have a great contract opportunity for a Process Development Sr Scientist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 3 years of experience in construction management/engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT – KEY RESPONSIBILITIES: Analytical method troubleshooting, qualification, validation, bridging, transfer. Analytical support for Process Development and Process Qualification activities. Understanding data flow in laboratory systems and data integrity. Ensure timely completion of Laboratory Investigations, Deviations, PMAFs. Participate in internal/external audits/inspections as required. Plan and implement procedures and systems to maximize operating efficiency. Manage and contribute to the achievements of department productivity and goals. Engage with the Continuous Improvement Process. ABOUT YOU – ARE YOUR SKILLS A MATCH? Third level qualification (Degree) in Analytical Chemistry/ Biochemistry or related discipline. Have 3-6 years of relevant analytical experience in the Pharmaceutical Industry. Subject Matter Expert for General and Compendial methods used in the analysis of Drug Product such as Sub Visible Particle Analysis, KF Moisture, Ph, Osmolality, Density, App/Colour/Clarity, CCI, Breakloose and Extrusion, RAMAN, FTIR, NIR, UV/VIS Spectrophotometry, SEM. Experience with Chromatographic methods such as HPLC, UPLC, with UV, RID, Mass Spec detection. Experience with developing, validating, troubleshooting, analytical methods. 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 note that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Gráinne Hodnett on 021 4777 329 if you have any more questions about this opportunity! #J-18808-Ljbffr
Associate Quality Specialist (Shift) (BBBH28026) Cork, Republic of Ireland LSC have a great contract opportunity for an Associate Quality Specialist to join a global Biopharmaceutical company in Cork. The facility specializes in the fermentation, purification, and sterile filling of biotech products, as well as supporting product development and clinical trials. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Provides to the site expertise in Quality Systems and/or Operational Quality, including the following i.e. Quality Notifications/Investigations/ Change Management; environment monitoring programs; sterility assurance/low bioburden manufacturing; etc. Uses knowledge to improve Quality Systems and/or Operational Quality; solve complex problems, provide continuous improvement and execute tasks. Required to be proficient in Quality approval and oversight for Commissioning and Qualification activities (IQ/OQ/PQ) Provides compliance contribution to project teams and leads small projects. Coaches and guides colleagues within the site. Participation in inspections of Site by Divisional / Regulatory Bodies / third parties together with follow up actions where applicable. Deviation Management & Change Control approval. Champion the highest Quality and Compliance standards for the site. ABOUT YOU - ARE YOUR SKILLS A MATCH? Degree or 3rd level qualification (Science, Quality). Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation. 5 years’ experience in the pharmaceutical industry or a similar operating environment which includes experience in a Quality function. Quality Assurance SME knowledge, from both operational and educational experience, is required. Advanced PC skills such as Excel, Word, PowerPoint. Stakeholder management of multiple decision makers, auditors, cross functional teams by demonstrating the ability to maintain and strengthen trust relationships with people on all levels. 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 Grainne Hodnett @ 0214777329 if you have any more questions about this opportunity! #J-18808-Ljbffr
