Automation Engineer – Mullingar (On-site) Medical Device Manufacturing | Injection Moulding I’m currently partnering with a leading and highly reputable manufacturer in the medical device sector to recruit an Automation Engineer for their site in Mullingar. This is an excellent opportunity to join a high-performing engineering team within a regulated, high-volume production environment. The Opportunity This is a hands‑on role focused on maintaining, optimising, and improving automated injection moulding systems. You will play a key part in ensuring efficient production and consistent quality in line with strict regulatory standards. Key Responsibilities Install, maintain, and troubleshoot automated manufacturing equipment, including robotics and control systems Perform fault‑finding across electrical, mechanical, pneumatic, hydraulic, and PLC systems Execute preventative and corrective maintenance to minimise downtime Support commissioning, validation, and integration of new equipment Collaborate on new product introductions (NPI) and continuous improvement initiatives Work with external vendors on installations, upgrades, and validations Maintain accurate maintenance documentation in line with regulatory requirements Ensure compliance with safety, quality, and environmental standards including ISO 13485 and GMP Contribute to root cause analysis and implement corrective actions What We’re Looking For Level 6 qualification or higher in Electrical, Automation, Mechatronics, or similar Minimum 2 years’ experience in an automated manufacturing environment Strong PLC knowledge such as Allen Bradley, Siemens, or similar Experience with robotics, sensors, and vision systems Proven troubleshooting skills across electrical and mechanical systems Understanding of pneumatic and hydraulic systems Ability to read technical drawings and schematics Strong problem‑solving skills and attention to detail Ability to work both independently and as part of a team Nice to Have Experience in medical devices, pharma, or other regulated industries Exposure to validation processes such as IQ, OQ, PQ Familiarity with lean manufacturing and continuous improvement If you are interested in learning more, feel free to reach out directly or apply via LinkedIn. All conversations will be handled with strict confidentiality. #J-18808-Ljbffr
Russell Tobin is currently seeking an Associate Scientist to join a dynamic MS&T Process Analytics team in Dublin, Ireland. The role involves executing analytical methods, providing support for process characterization, and partnering with QC teams to solve technical issues. Ideal candidates will possess a BSc, MSc, or PhD in a relevant field along with hands-on experience in the biopharmaceutical sector. This position offers the chance to work in a fast-paced and collaborative biologics manufacturing environment. #J-18808-Ljbffr
We are currently seeking an Associate Scientist to join a dynamic MS&T Process Analytics team supporting biologics drug substance operations within a fast-paced pharmaceutical manufacturing environment. Key Responsibilities Execute analytical methods and support troubleshooting, remediation, and optimization activities Provide analytical support for process characterization studies Partner with QC teams to investigate and resolve technical issues Support development, qualification, and transfer of analytical methods Review method performance and assist with continuous improvement initiatives Collaborate cross‑functionally with teams across multiple sites to ensure method readiness and performance in a commercial environment Key Requirements BSc, MSc, or PhD in Biological Sciences, Chemistry, Biotechnology, or a related discipline Experience within biologics, biopharmaceutical, or analytical development environments Hands‑on experience with analytical techniques such as HPLC, ELISA, electrophoresis, spectrometry, etc. Knowledge of method qualification/validation and cGMP laboratory practices Strong troubleshooting, communication, and collaboration skills This is an excellent opportunity for candidates looking to gain experience in a highly collaborative and technically advanced biologics environment. #J-18808-Ljbffr
Document Controller | Dublin, Ireland | Contract We're recruiting on behalf of a confidential client, a major pharmaceutical organisation, for an experienced Document Controller to join a significant, site-based capital project in Dublin. This is a fully embedded, client-side role at the heart of a complex, multi-phase project environment. This is a rare opportunity to work directly within an owner's project team on a flagship Irish pharma capital project, with full visibility across design, construction, CQV and handover phases. The Role Own and manage all client-side project documentation across the full project lifecycle Control document receipt, review, approval, issue, revision control and archiving Act as the primary interface with EPCM partners, vendors, contractors and internal stakeholders on all documentation matters Ensure all documentation adheres to GMP standards, data integrity requirements and ALCOA+ principles Maintain accurate document registers, trackers and status reporting Support CQV documentation, executed protocols and final turnover packages to operations Assist with audits, inspections and project close-out activities What You\'ll Bring Proven track record as a Document Controller on pharmaceutical or life sciences capital projects Hands-on, working experience with EIDA Previous experience embedded within a client-side or owner's project team Strong working knowledge of GMP documentation requirements Experience supporting construction, commissioning and qualification documentation workflows Ability to commit to a full-time, fully on-site role in Dublin Advantageous Experience Background on large-scale Irish pharma projects, drug product, biologics or sterile manufacturing facilities Familiarity with validation platforms such as ValGenesis, Kneat or ACC Interested? Lets talk. The client is looking to move quickly. If you have the EIDA experience and a strong pharmaceutical capital projects background, I'd love to hear from you, even if you'd prefer a confidential conversation before committing to a formal application. Drop me a message, apply below, or send your CV directly. All applications treated in strict confidence. #J-18808-Ljbffr
QC Instrumentation Engineer (12-Month Contract) We are currently seeking a QC Instrumentation Engineer to join a leading biopharmaceutical manufacturing site in Dublin 15 on a 12-month contract. This is an excellent opportunity to work within a high-performing Quality Control environment, supporting critical laboratory instrumentation and ensuring compliance with GMP standards. Key Responsibilities Manage the purchase, installation, qualification, and lifecycle of QC laboratory instruments Provide calibration and maintenance services, including scheduling and tracking activities Review and approve documentation related to instrument qualification, calibration, and repairs Lead and manage instrument‑related investigations, including calibration deviations Trend and monitor instrument performance and lifecycle dataSupport new instrument introduction and qualification projects Collaborate with cross‑functional teams including QC, QA Validation, and CSV Liaise with vendors and global stakeholders on instrumentation activities Ensure compliance with GMP, Data Integrity (21 CFR Part 11 / EU Annex 11) and internal procedures Contribute to the development and improvement of instrumentation procedures Troubleshoot complex instrumentation issues within the QC laboratory Qualifications B.Sc in a scientific discipline (or related field) Minimum 3 years experience in a GMP environment At least 1 year of hands‑on instrument qualification experience Strong understanding of laboratory instrumentation lifecycle management Knowledge of Data Integrity requirements (21 CFR Part 11 / EU Annex 11) Familiarity with biopharmaceutical drug substance and drug product testing Understanding of protein biochemistry Experience supporting technology transfers What We’re Looking For Strong team player with the ability to collaborate across functions Excellent organisational and time management skills Ability to manage multiple priorities and projects simultaneously Clear and effective communication skills #J-18808-Ljbffr
Russell Tobin is seeking an experienced Microbiologist to join a leading pharmaceutical organization in Dublin, Ireland. The role involves supporting manufacturing operations through environmental monitoring and in-process testing. Candidates should have a Level 8 degree in Microbiology and at least 2 years' experience in a related laboratory setting. The position offers a dynamic work environment with opportunities to utilize cutting-edge laboratory technologies and make a significant impact on patient outcomes. #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
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
Exciting Opportunity | Microbiologist | Leading Pharmaceutical Organisation | Ireland Are you an experienced Microbiologist looking to take your next step within a world-class pharmaceutical environment? We are partnering with a leading pharmaceutical manufacturer to identify a talented Microbiologist to join their growing Quality Control team. This is a fantastic opportunity for a driven scientific professional who thrives in a fast-paced, highly regulated cleanroom environment and wants to be part of a team that genuinely impacts patient outcomes. The Role As a Microbiologist, you will play a critical role in supporting manufacturing operations through environmental monitoring, in-process testing, and aseptic qualification activities. Day-to-day, you can expect to be involved in: Cleanroom, BSC & Isolator batch-related environmental monitoring Utility sampling of water systems and Compressed Air/Gas In-process testing using HPLC and UV Spectrophotometry Issuance, receipt, and testing of Biological Indicators (BIs) Reconciliation, inspection, and active participation in Media Fills (APS) Microorganism identification post-testing Investigation of alert/action limit excursions Receipt and processing of drug substance and drug product samples Supporting documentation authoring, review, and GMP compliance Please note: This role may involve shift pattern working. What We're Looking For Minimum Level 8 degree in Microbiology or a related discipline At least 2 years' experience in a pharmaceutical, healthcare, or related technical laboratory setting Hands-on experience in a cleanroom environment using aseptic techniques Isolator experience is a strong advantage this is a key focus of the role Experience with HPLC and UV Spectrophotometry is desirable Familiarity with systems such as MODA, Empower, LIMS, CIMS, LES, or Veeva Vault is a plus Strong written and verbal communication skills A collaborative team player with a proactive mindset Key Differentiators We're Screening For Compressed Air/Gas utility sampling experience Isolator batch monitoring Biological Indicator testing Media fill participation (APS) If you tick these boxes, we want to hear from you! What's On Offer A role with genuine scope and variety within a regulated pharmaceutical setting The opportunity to work with cutting-edge laboratory technologies Interested? Send your CV directly via LinkedIn or reach out for a confidential conversation. #J-18808-Ljbffr
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. 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
