Snr Associate - Contract Development and Manufacturing Our client is seeking a candidate to join the External Supply Manufacturing team initially for a 12-month period. The successful candidate will need to be living in Ireland while also being fully eligible to work in Ireland. This role works in partnership with different departments & stakeholders to ensure a smooth manufacturing process and compliance with quality standards. The role also requires applying process, operational, and scientific expertise, as well as basic compliance knowledge and analytical and troubleshooting abilities, to support quality records. Responsibilities Strong understanding of GMP pharmaceutical manufacturing environments , including API, Drug Substance, Drug Product or Packaging operations. Experience managing quality systems and records , including deviations, CAPAs, change controls and investigation documentation. Ability to perform root cause investigations and implement effective corrective and preventative actions to prevent recurrence. Experience working with or supporting third-party manufacturing partners or CDMOs , ensuring compliance with internal quality standards and procedures. Strong capability in data analysis and performance monitoring , including reviewing manufacturing metrics and identifying opportunities for operational improvement. Excellent technical writing and documentation skills , with the ability to clearly communicate complex technical information. Strong problem-solving and critical thinking skills in regulated pharmaceutical environments. Experience working collaboratively across cross-functional teams , including quality, manufacturing, supply chain and external partners. Proficiency in QMS and digital systems , such as Veeva Vault, TrackWise or similar quality management platforms. Advanced working knowledge of Microsoft Office tools , particularly Excel, PowerPoint, Project, Visio and Smartsheet. Basic Qualifications Bachelor's Degree (L8) in Business Administration, Engineering or Science-related field, with 2+ years of experience in GMP protein, API, DS, DP or packaging manufacturing environment Experience in roles requiring knowledge of cGMP principles, FDA and other regulatory agency guidelines, and validation principles Understanding of applicable manufacturing/testing processes (i.e. protein, API, Drug Substance, Drug Product, Packaging, Device manufacturing processes) Strong technical background with understanding of pharmaceutical manufacturing, commercialisation, and cGMP knowledge / experience. Problem-solving, critical thinking and decision-making skills. Demonstrated negotiation skills, accountability to deliver results and meet deadlines while handling contending priorities. Technical writing and multi-level communication skills. Demonstrated ability to perform effectively in a collaborative/team environment. Demonstrated ability to take initiative, drive action, and work under minimum supervision. #J-18808-Ljbffr
A leading recruitment firm is seeking a talented Cloud Software Engineer for a hybrid role in Dublin. The successful candidate will design, implement, and maintain innovative cloud solutions. Key responsibilities include writing clean code, unit testing, and collaborating with cross-functional teams. Candidates should have strong experience with Terraform and public cloud platforms such as AWS, Azure, or GCP. Additional skills in programming languages like Java, Python, and Go are essential. This is an exciting opportunity to work with cutting-edge technologies. #J-18808-Ljbffr
Cloud Software Engineer Dublin Ireland (Contract Hybrid 3 days a week onsite in South Dublin) My clients are looking for a talented Cloud Software Engineer to join our team and help deliver innovative cloud solutions aligned with our bank's cloud strategy. You will design, implement, and maintain scalable software solutions while collaborating across development, QA, and project management teams. This is a fantastic opportunity to work with cutting‑edge cloud technologies, Infrastructure as Code, and cloud security frameworks. Key Responsibilities Design and implement new software solutions as part of our cloud enablement strategy Maintain and enhance existing software systems Write clean, secure, and performant code adhering to best practices Conduct unit and integration testing Participate in requirements gathering, architecture reviews, and design discussions Work collaboratively in cross‑functional teams to deliver high‑quality solutions Required Skills & Experience Strong experience with Terraform (Enterprise, Private Module Registry, Sentinel) and Infrastructure as Code Hands‑on experience with public cloud platforms (AWS, Azure, or GCP) Deep knowledge of distributed systems, web protocols, operating systems, and virtualization Experience with cloud security tools and frameworks (Azure Policy, Defender for Cloud, Sentinel) Proficiency in programming languages: Java, Python, Go Experience with CI/CD pipelines (e.g., Maven, Jenkins) Knowledge of container technologies (Docker, Kubernetes, OpenShift) Familiarity with configuration management and automation tools: Ansible, Puppet, CloudFormation, Salt Experience in Linux/UNIX system administration Cloud certifications (e.g., AWS Certified Developer, AWS Solutions Architect) are a plus Agile development and test‑driven development (TDD) experience #J-18808-Ljbffr
A reputable staffing agency seeks a Senior Associate for Contract Development and Manufacturing based in Dublin, Ireland. This role involves managing quality systems, conducting root cause investigations, and collaborating across teams in a regulated GMP environment. Candidates should have a Bachelor's Degree and a solid foundation in pharmaceutical manufacturing processes. Strong analytical, problem-solving, and communication skills are essential. This is an excellent opportunity for someone looking to advance their career in the pharmaceutical industry. #J-18808-Ljbffr
Global Biotechnology company based in south Dublin, Ireland - looking for QC Senior Associate . The successful candidate will be responsible for one or more of the following activities in QC including sample and data management and equipment maintenance. This role will support QC and manufacturing operations, as some extended hours and weekend work flexibility may be necessary as required. The Job Execute sample management activities across the site - sample distribution, LIMS logging, shipment receipt. Perform Stability Program related activities such as pulling stability samples and study initiations. Create/own and approve protocols, sample plans., SOPs, training manuals. Perform SAP, LIMS and CIMS functions/ transactions within the sample management remit Out-of-hour responder for sample management equipment (fridges /freezers / incubators) Responsible for their own training and safety compliance. Sample shipments and temperature monitoring activities. LIMS data coordination of commercial and import batches. Management and maintenance of the Site Inventory of Reference Standards, Assay Controls, Training and Verification samples. QC Representative for NPI activities and routine Product meetings as required. Have You Bachelor's degree in a Science related field is required. 4+ years of bio-pharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, where 2 - 3 years of specific sample management/ stability program experience is desirable. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Working knowledge of aseptic compliance within the manufacturing environment and demonstrated leadership and communication skills to communicate requirements to colleagues. Auditing documentation and operation process. Demonstrated ability to interact with regulatory agencies. The successful candidate must have eligible working VISA in Ireland or European Union (EU) passport. Berkley Life Science & Engineering is a specialist consultancy, recruiting professionals for organizations throughout Ireland, UK & Europe; for more information go to www.berkley-group.com If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone Aleksas Kremenskas at +353 (0) 87 2727949 or send your profile to akremenskas@berkley-group.com #J-18808-Ljbffr
A leading architectural firm is seeking a qualified Architectural Technologist in Dublin, Ireland. The successful candidate will work on diverse Pharmaceutical and Life Science projects across Ireland and Europe. Key requirements include a minimum of 6 years of post-graduate experience, proficiency in BIM/Revit, and strong design and communication skills. Familiarity with Irish Planning and Building Regulations is also essential. The role involves collaboration within a project manager-led team, emphasizing technical and design capabilities. #J-18808-Ljbffr
A global pharmaceutical company based in Dublin is seeking a Specialist Manufacturing to manage complex deviation investigations and lead cross-functional teams. The ideal candidate will have a Bachelor's degree in Science or Engineering, with over 5 years of relevant experience in biotech or pharma manufacturing. Strong technical writing skills and an understanding of fill/finish operations are essential. This role involves presenting findings to regulatory inspectors and driving continuous improvement efforts in the investigation process. #J-18808-Ljbffr
We are looking for an experienced Maintenance Supervisor for a busy food production facility. This is a hands‑on role requiring strong mechanical skills, with responsibility for supervising a small team of operators, fitters, and technicians across multiple production lines. Key Responsibilities Lead and coordinate a team of 7 maintenance staff, providing guidance, training and support. Carry out hands‑on mechanical maintenance and troubleshooting of production machinery. Plan and schedule maintenance work to ensure smooth and efficient operations. Conduct safety inspections and ensure compliance with health and safety standards. Maintain accurate asset registers and preventative maintenance schedules. Manage tools, equipment, and spare parts procurement. Provide expert advice and solutions to complex mechanical or operational issues. Ideal Candidate Strong mechanical fitting background with proven hands‑on experience. Previous supervisory experience in a production or manufacturing environment. Familiarity with food production machinery, including refrigeration units, conveyors, timing belts, and processing/filling equipment. Experience in food processing or similar manufacturing industries is highly desirable. Able to work in a fast‑paced environment and manage multiple priorities effectively. This is a unique opportunity to join a dynamic production team, taking ownership of machinery maintenance while developing and leading a skilled team. If you are interested please send your cv to jbarron@berkley-group.com #J-18808-Ljbffr
A specialist consultancy is seeking an experienced industrial electrician in Cork. The successful candidate will handle electrical installation, maintenance, and troubleshooting on pharmaceutical sites. Essential qualifications include a National Craft Certificate or equivalent and 3-5 years of hands-on experience in regulated environments. Flexibility for shift work and travel is required. This role emphasizes safety and documentation skills in compliance with GMP standards. #J-18808-Ljbffr
A leading project management consulting firm is seeking an experienced Dual Design Project Manager to support creative and design initiatives in Cork. The ideal candidate will have at least 5 years of experience in project management, focusing on coordination across global teams. Responsibilities include managing project timelines, resources, and stakeholder communication. This role offers a hybrid work model, combining onsite collaboration with flexible remote work, with a PAYE contract starting at €47,000 per annum. #J-18808-Ljbffr
