A leading biotech company in County Clare, Ireland is seeking a QC Specialist to support GMP-compliant activities in Quality Control for gene therapy products. This role involves a variety of responsibilities from equipment qualification to routine testing, promoting communication and data integrity. Suitable candidates must have a degree in Human Health or Sciences, at least 8 years in the pharma or biotech industry, and knowledge of GMP regulations. Strong analytical and communication skills are essential. #J-18808-Ljbffr
Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward! R&D Partners is seeking a Formulation Scientist to join our client's Inhalation Product Development team. This role is perfect for someone who enjoys hands-on work in pharmaceutical formulation, particularly in creating and scaling up batches. You will oversee batch manufacturing activities, assist with regulatory submissions, and help develop reliable processes for producing inhalation products like Metered Dose Inhalers (MDIs) and Dry Powder Inhalers (DPIs). Please note that to be considered for this role you must have the right to work in this location Responsibilities Prepare and execute small-scale and larger-scale batches, ensuring accuracy and proper documentation. Assist in producing batches for stability testing, clinical trials, or regulatory submissions. Help design and improve manufacturing processes for commercial production. Work closely with the lead formulator to plan experiments and achieve technical goals. Analyze and interpret data using scientific methods and statistical tools. Maintain detailed records of all development work and contribute to technical reports. Support the creation of batch records, protocols, material specifications, and regulatory documents. Troubleshoot formulation or process challenges during development or scale-up. Follow Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and company policies. Apply Quality by Design (QbD) principles throughout the development process. Key Skills and Requirements A degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field. Hands-on experience in pharmaceutical formulation or process development. Familiarity with inhalation products (MDI/DPI) is a plus but not required. Strong skills in analyzing data, writing reports, and maintaining documentation. Ability to work independently and collaboratively in a fast-paced environment. Adaptable, proactive, and detail-oriented. For more information, please contact Timi Asseez . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. #J-18808-Ljbffr
Join a leading biotech in Ireland as a Bioprocessing Scientist powering GMP-grade productions in a cutting-edge cleanroom. R&D Partners is seeking a Bioprocessing Scientist to join a leading biotechnology company in Ireland. This role focuses on performing production processes in a GMP-compliant cleanroom environment while ensuring compliance with health and safety standards. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Execute production processes using aseptic techniques in a GMP-compliant cleanroom. Monitor and maintain facility cleanliness, safety, and environmental standards. Review and update process documentation and perform routine equipment checks. Manage stock inventory, including ordering, receiving, and storing materials. Identify and report deviations, support investigations, and assist with technology transfers. Ensure timely delivery of products while adhering to health and safety procedures. Key Skills and Requirements Execute production processes using aseptic techniques in a GMP-compliant cleanroom. Monitor and maintain facility cleanliness, safety, and environmental standards. Review and update process documentation and perform routine equipment checks. Manage stock inventory, including ordering, receiving, and storing materials. Identify and report deviations, support investigations, and assist with technology transfers. Ensure timely delivery of products while adhering to health and safety procedures. #J-18808-Ljbffr
A leading pharmaceutical company in Ireland seeks a Formulation Scientist to join their Inhalation Product Development team. This role involves hands-on work in pharmaceutical formulation, overseeing batch manufacturing, assisting with regulatory submissions, and developing reliable processes for inhalation products like MDIs and DPIs. The ideal candidate has a degree in Pharmaceutical Sciences or a related field, with strong skills in data analysis and documentation. An adaptable, detail-oriented approach is essential for working in this fast-paced environment. #J-18808-Ljbffr
Safeguard the quality behind life‑changing gene therapies through GMP‑driven QC excellence. R&D Partners is seeking a QC Specialist to support GMP-compliant activities within Quality Control (QC) for the manufacture and release of plasmids and gene therapy products. This role involves contributing to a GMP facility for gene therapy production, with responsibilities spanning equipment qualification, method transfer, routine in-process and release testing, and other QC-supporting activities. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Support technical transfer of drug substance dilution to QC. Conduct bridging studies for QC dilutions to compare dilution regimes. Execute dilution studies, including equipment installation and qualification. Plan, track, monitor, and execute QC stability studies in accordance with international standards and regulations. Address issues, CAPAs, change controls, action items, and risk assessments within QC. Escalate and resolve QC issues with site leadership. Lead major investigations impacting QC analysis. Author and review scientific and technical documentation. Stay updated on developments in methods and regulations for ATMP analytics. Promote effective communication within the team, across departments, and with external collaborators. Ensure data integrity throughout the data lifecycle. Maintain compliance with GMP, GDP, and GxP guidelines. Support new product introductions and strategic QC-related activities. Key Skills and Requirements Analytical Skills: Ability to synthesize complex information and use data-driven insights. Problem Solving: Timely resolution of issues with alternative solutions. Leadership: Inspire and motivate others while accepting feedback. Cost Consciousness: Work within budgets and implement cost‑saving measures. Planning & Organization: Prioritize tasks and manage time efficiently. Professionalism: Treat others with respect and maintain composure under pressure. Quality Management: Promote quality improvements and ensure accuracy. Communication: Strong oral and written communication skills, including technical writing. Qualifications Degree in Human Health or Sciences, or equivalent relevant work experience. Minimum 8 years of experience in the pharmaceutical or biotech industry. Demonstrated knowledge of GMP environments and quality control. Experience with audits and client-facing interactions. Proficiency in EU/FDA regulations, ICH guidelines, GMP/GLP/GCP, Lean Manufacturing, and Six Sigma. Strong collaboration, communication, and conflict resolution skills. #J-18808-Ljbffr
A leading pharmaceutical innovation firm in Ireland is looking for a QC Laboratory Manager to lead quality control operations at an inhalation site. This role requires overseeing laboratory activities, ensuring compliance with regulatory standards, and contributing to the strategic growth of the site. The ideal candidate will have a degree in Chemistry or a related field, experience in a pharmaceutical laboratory, and strong leadership abilities. Join us to make a meaningful difference in developing life-changing treatments. #J-18808-Ljbffr
A leading biotech company in Ireland seeks a Bioprocessing Scientist to conduct production processes in a GMP-compliant cleanroom. The role includes maintaining safety standards, reviewing documentation, and managing inventory. Ideal candidates will have experience with aseptic techniques and understand health and safety procedures. This position offers the chance to work in an innovative environment dedicated to quality and efficiency. #J-18808-Ljbffr
Ready to oversee a laboratory thats bringing life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference! R&D Partners is seeking a QC Laboratory Manager to oversee quality control operations at an inhalation site. This role involves leading laboratory activities, ensuring compliance with regulatory standards, and supporting the strategic growth of the site. You will work closely with cross‑functional teams to enhance processes and develop leadership within the quality control team. Please note that to be considered for this role you must have the right to work in this location. Responsibilities Develop and implement testing processes and infrastructure. Lead laboratory design, setup, and team management. Oversee changes to methods and specifications, ensuring compliance. Manage investigations, technical transfers, and contract laboratory testing. Collaborate with regulatory departments and authorities to meet compliance requirements. Work with various departments to ensure smooth operations and maintain standards. Support leadership development within the quality control team. Contribute to the strategic expansion of the lab's capabilities and operations. Identify and implement process improvements to enhance efficiency and resource management. Key Skills and Requirements Degree in Chemistry or a related field. Experience in a pharmaceutical laboratory environment. Leadership experience in managing teams and projects. Strong organizational and time management skills. Excellent communication and presentation abilities. Familiarity with conducting internal audits and maintaining compliance records. Eligibility to work in Ireland. #J-18808-Ljbffr
A leading biotechnology company in Ireland is looking for a Technical Bioprocessing Scientist to support GMP manufacturing operations. This role entails coaching team members, ensuring compliance with GMP standards, and driving continuous improvement initiatives. The ideal candidate should have strong knowledge of GMP standards, experience managing GMP documentation, and excellent communication skills. This position is crucial for enhancing operational excellence within bioprocessing operations. #J-18808-Ljbffr
Keep pharmaceutical operations running flawlessly through smart, compliant, and efficient maintenance planning. R&D Partners is seeking a Maintenance Planner to oversee and organize maintenance activities at a pharmaceutical or biopharmaceutical site. You will work closely with technicians, engineers, vendors, and other teams to ensure maintenance tasks are planned, scheduled, and completed efficiently while meeting regulatory standards. This role requires strong organizational skills, technical knowledge, and the ability to collaborate across various departments. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Plan and schedule maintenance tasks, including inspections, repairs, and calibrations, using SAP systems. Assess maintenance needs and determine appropriate actions in collaboration with engineers, technicians, and quality assurance teams. Coordinate maintenance schedules with production planning and other stakeholders to minimize disruptions. Manage spare parts and tools inventory using SAP systems. Maintain accurate records of maintenance activities, analyze data, and update procedures for continuous improvement. Review and approve maintenance work orders and ensure compliance with regulatory standards. Participate in the implementation of global SAP systems, including testing, training, and updating procedures. Act as a representative for maintenance and calibration during audits and inspections. Key Skills and Requirements: Familiarity with SAP S-4HANA, specifically SAP EAM (Enterprise Asset Management). 5+ years of maintenance experience within a life sciences manufacturing facility. Knowledge of mechanical and electrical systems, calibration equipment, and maintenance strategies. Strong communication, coordination, and problem‑solving skills. Ability to prioritize tasks and work collaboratively with cross‑functional teams. Educational background in Engineering, Science, or a related technical field. For more information, please contact Billy O'Brien. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/ #J-18808-Ljbffr
