A leading pharmaceutical organisation is seeking a QA Specialist in Dublin to support day-to-day quality activities and compliance. The role involves collaborating with cross-functional teams to maintain and improve quality standards. Candidates should have a degree in a scientific discipline and experience in a QA role. Strong attention to detail and organisational skills are essential. Opportunities for professional development are available in this collaborative environment. #J-18808-Ljbffr
I’m currently partnering with a leading pharmaceutical organisation to recruit a QA Specialist to join their growing quality team in Dublin. This is an excellent opportunity for a quality professional looking to work in a regulated, fast‑paced environment, supporting key quality systems and ensuring compliance across operations. The Role As a QA Specialist, you will support day‑to‑day quality activities across manufacturing and quality systems, helping to ensure products are developed, tested, and released in line with regulatory expectations. You’ll collaborate with cross‑functional teams and play an important role in maintaining and improving the organisation’s quality standards. Key Responsibilities Support quality systems including deviations, investigations, and CAPA management Review and approve GMP documentation and records Assist with internal audits and regulatory inspections Ensure compliance with cGMP requirements across operations Support document control and quality system improvements Provide QA guidance to operational teams Contribute to training and continuous improvement initiatives About You Degree in a scientific or related discipline Experience in a QA role within the pharmaceutical or life sciences industry Good understanding of cGMP requirements Strong attention to detail and organisational skills Ability to manage multiple priorities in a fast‑paced environment Effective communicator with a collaborative approach Why Apply? Join a well‑established pharmaceutical organisation Gain exposure to a broad range of QA activities Work in a collaborative and quality‑driven environment Opportunities for professional development and growth #J-18808-Ljbffr
We are currently working with a leading organisation in the regulated manufacturing sector to recruit a Maintenance Technician to join their established Maintenance and Process Control Centre (MPCC) team. This role will focus on ensuring equipment reliability, executing planned maintenance activities, and responding to equipment failures in a highly regulated manufacturing environment. The successful candidate will work closely with cross-functional teams including Operations, Quality, and Engineering, supporting reliability‑centred maintenance activities across the facility. Key Responsibilities Identify workplace risks and implement appropriate mitigation actions to maintain a safe working environment. Respond promptly to equipment failures and issues in a cross‑functional environment, ensuring minimal disruption to operations. Record all interventions including failure codes and provide guidance for preventative action where required. Execute planned maintenance routines including predictive, preventative, and calibration activities. Complete all Work Orders on time in a safe and compliant manner, ensuring accurate asset management data capture. Provide clear written and verbal handovers to colleagues across shifts and departments. Participate in continuous improvement initiatives and identify enhancements to job plans and spare parts management. Support major equipment overhauls and manage vendor activities when on site. Develop training materials and cross‑train colleagues to build team capability. Assist with operational activities including set‑up, sampling, and cleaning validation tasks. Work within cross‑functional teams using Operational Excellence techniques to optimise processes. Maintain audit‑ready standards, uphold housekeeping expectations, and complete training on schedule. Qualifications and Experience FETAC Level 6 Electrical qualification or equivalent with demonstrated mechanical aptitude. Minimum 3 years experience in a maintenance or engineering role within a regulated manufacturing environment. Experience in biopharmaceutical, pharmaceutical, medical device, facilities maintenance, or FMCG sectors is essential. Strong commitment to safety, quality, and reliability in all tasks. High attention to detail with ability to follow procedures accurately. Flexibility and openness to change in a dynamic manufacturing environment. Ability to work independently and collaboratively within a team setting. Strong problem‑solving skills with ability to adhere to scheduled timelines. Why Apply Day shift schedule Monday to Friday, supporting work‑life balance. Opportunity to work with advanced equipment and technology in a regulated environment. Continuous improvement culture with ongoing training and development opportunities. Collaborative, cross‑functional team environment focused on operational excellence. Next Steps If you are interested in learning more about this opportunity, please apply directly or contact me for a confidential discussion. #J-18808-Ljbffr
A leading organisation in regulated manufacturing is seeking a Maintenance Technician to join their Maintenance and Process Control Centre team. This role emphasizes ensuring equipment reliability, executing planned maintenance, and responding to equipment failures in a highly regulated environment. The ideal candidate will have a FETAC Level 6 Electrical qualification or equivalent, with a minimum of 3 years experience in maintenance or engineering roles. The position offers a day shift schedule and opportunities for ongoing training and development in a collaborative environment. #J-18808-Ljbffr
Scientist, Manufacturing Technology Dublin | On-site | 12-month contract I am currently working with a leading global biopharmaceutical organisation to recruit a Manufacturing Technology Scientist to support a Multi-Product Cell Culture (MPCC) commercial manufacturing facility based in Dublin. This role sits within the Manufacturing Technology group, which is responsible for process validation and continued technical support of cell culture, primary recovery, and downstream unit operations supporting the commercial manufacture of multiple mammalian cell processes. The successful candidate will be a key contributor to a highly technical and collaborative site and global team. Key Responsibilities Provide process subject matter expertise for drug substance manufacturing, with strong knowledge of downstream operations including buffer preparation, chromatography, purification, viral inactivation and viral reduction filtration, ultrafiltration, formulation, and bulk fill. Working knowledge of upstream operations is beneficial, including media preparation, large-scale cell culture, scale-up, single-use systems, bioreactors, and harvest clarification. Author and review technical documentation such as protocols, reports, and SOPs to support process validation and lifecycle management. Generate and execute commercial-scale technical and plant-supporting studies on the manufacturing floor. Provide on-the-floor manufacturing support, including troubleshooting processing issues and leading investigations into process deviations. Identify and implement process improvements related to yield, robustness, and cycle time using data-driven approaches. Support regulatory inspections and interactions, representing the site as a process and technical subject matter expert. Communicate technical learnings effectively across internal and external forums. Participate in change control, CAPA, and continuous improvement or Lean initiatives. Qualifications and Experience BSc or equivalent in a scientific or engineering discipline. Minimum of 5 years’ experience in drug substance manufacturing technical support within the biopharmaceutical industry. Strong understanding of cGMP compliance and regulatory agency requirements. Excellent technical writing and verbal communication skills. Demonstrated ability to work effectively in cross-functional and global matrix environments. Ability to develop, present, and defend scientific and technical approaches. Proven capability to influence stakeholders without direct line authority, balancing product quality and operational requirements. Additional Information This is an on-site role requiring physical presence at the manufacturing facility. The position may occasionally require extended hours, modified work schedules, or on-call availability. Why Apply Opportunity to work at commercial scale in a highly advanced multi-product biologics manufacturing facility. Strong exposure to cross-functional teams including Manufacturing, Quality, Engineering, and Regulatory groups. Hands-on technical role with direct impact on process performance, product quality, and continuous improvement. #J-18808-Ljbffr
A leading global biopharmaceutical organisation in Dublin is seeking a Manufacturing Technology Scientist for a 12-month on-site contract. This role involves providing technical expertise in downstream operations, authoring technical documentation, and supporting regulatory inspections. Candidates should have a BSc in a relevant field and at least 5 years of experience in drug substance manufacturing. There is an opportunity for hands-on technical work within a collaborative environment, directly impacting process performance and quality. #J-18808-Ljbffr
Hiring: Manufacturing Support Scientist/Engineer (NPI) – 12 Month Contract We are currently seeking a Manufacturing Support Scientist/Engineer to join a high-performing biologics manufacturing team, supporting New Product Introduction (NPI) activities in a fast-paced GMP environment. This is an exciting opportunity to play a key role in bringing new biologics products into commercial manufacturing, working cross-functionally to ensure robust, efficient, and compliant processes. Collaborate with cross-functional teams (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain) to support new product introductions, process improvements, and change initiatives Support risk assessments to ensure appropriate controls are in place for manufacturing readiness Contribute to technology transfer activities , including preparation of documentation for development, engineering, and PPQ batches Lead and support change controls, CAPAs, deviations, and investigations Develop process impact assessments and support product changeover strategies Act as a manufacturing representative to ensure end-user requirements are captured Drive process improvement projects and support implementation through to completion Provide SME input into process optimization, procedures, and documentation updates Support audit readiness (internal and external) Deliver training and knowledge transfer to operations teams Support the introduction of new raw materials, consumables, and technologies (e.g. single-use systems) Promote a Right-First-Time culture and apply lean manufacturing principles Approve GMP documentation including SOPs and electronic batch records Support sustaining operations as needed to ensure continuity of supply Qualifications & Experience Bachelor’s or Master’s degree (or near completion) in Science, Engineering, or a related discipline Strong understanding of GMP biologics manufacturing processes and equipment Experience supporting technical investigations and deviation closeout Working knowledge of systems such as DeltaV, MES (e.g. Syncade), and SAP Demonstrated problem-solving, project management, and organizational skills Excellent communication and stakeholder engagement abilities Experience in lean manufacturing / operational excellence is highly desirable Ability to thrive in a collaborative, fast-paced environment with changing priorities Strong team player with the ability to influence across functions Proactive mindset with a focus on continuous improvement High attention to detail with a commitment to quality and compliance Confidence in working across technical and operational teams #J-18808-Ljbffr
A prominent recruitment agency is seeking a Manufacturing Support Scientist/Engineer for a 12-month contract in Dublin, Ireland. This role involves supporting New Product Introduction activities in a fast-paced GMP environment, collaborating with cross-functional teams, and ensuring robust processes. The ideal candidate will hold a Bachelor’s or Master’s degree in a related discipline and possess strong problem-solving, communication, and project management skills. Familiarity with GMP processes and tools like DeltaV and SAP is essential. #J-18808-Ljbffr
