Global Supply Chain Planner – Actalent – Dublin Actalent is partnering with a client specializing in photopheresis technology. We are looking for a Global Supply Chain Planner who will act as the Subject Matter Expert (SME) for global direct and indirect procurement and planning activities, ensuring the timely and cost‑effective availability of materials and services necessary to support the company's worldwide operations. Responsibilities Plan and execute global direct and indirect procurement and direct and indirect planning activities to support worldwide operations. Experience & Qualifications Minimum 3 years experience in global procurement, production planning, or related roles. Experience with ERP systems. Supply planning and inventory management experience would be key for this role. Employment Type Contract – 12 month rolling contract, hybrid work in the Dublin office. Seniority Level Mid‑Senior level. Industries Hospitals and Health Care, Transportation, Logistics, Supply Chain and Storage, and Biotechnology Research. #J-18808-Ljbffr
Overview A leading pharmaceutical manufacturing site is seeking an Operations Specialist to support production activities in a cGMP environment. This role is ideal for someone with a strong technical background and a passion for continuous improvement. Type: Full-time | On-site | Day-based role with flexibility allowance Responsibilities Execute manufacturing operations in compliance with SOPs and batch records Support equipment installation, commissioning, and validation activities Assist with product demonstrations and validation for new product introductions Collaborate with Engineering, Quality, and other cross-functional teams Contribute to investigations, CAPAs, and change controls Train team members and support documentation updates Requirements Certificate-level qualification in Chemistry, Engineering, Biotechnology, or related field 2–3 years of experience in a cGMP commercial manufacturing environment Strong documentation and compliance skills Effective communication and teamwork abilities Familiarity with GMP utility systems (e.g., WFI, clean steam, pharmaceutical gases) is advantageous Ability to work independently and proactively Application If interested please apply! #J-18808-Ljbffr
We are seeking an experienced laboratory professional to lead strategic remediation and compliance initiatives in a regulated medical device environment. This role is critical to ensuring laboratory infrastructure, equipment, documentation, and practices meet global regulatory standards. Overview Key Responsibilities and Qualifications below outline the expectations for this senior role. Responsibilities Lead and execute laboratory remediation programs aligned with cGxP standards (ISO 13485, GLP, FDA QSR, GDP). Develop risk-based strategies for equipment qualification, calibration, and lifecycle management. Own CAPA and deviation processes, ensuring timely resolution and robust documentation. Author and approve SOPs, work instructions, and technical documentation in line with GDP and Data Integrity standards. Deliver training programs and mentor staff on compliant lab practices, equipment use, and safety. Collaborate with Engineering, QA, Facilities, and external service providers to support lab operations. Implement lean processes for inventory and procurement, and lead 6S and EHS initiatives. Qualifications Bachelor’s or Master’s degree in Engineering, Science, or related technical discipline. Minimum 10 years of experience in a regulated medical device or pharmaceutical laboratory. Strong knowledge of cGMP, GLP, GDP, ISO 13485, and EHS standards. Proven track record in leading remediation and compliance initiatives. Proficiency with Blue Mountain software. Excellent communication, organizational, and stakeholder management skills. Experience supporting audits and regulatory inspections. Six Sigma or Lean certification preferred. Seniority level Mid-Senior level Employment type Full-time Job function Quality Assurance Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Actalent by 2x Get notified about new Laboratory Technician jobs in Dublin, County Dublin, Ireland. Dublin 8, County Dublin, Ireland 1 day ago Dublin, County Dublin, Ireland 1 week ago Medical Laboratory Aide 0.50 WTE SCH0652025 Laboratory Assistant 1 (Permanent Wholetime) (Reference: 701a/2024) Dublin, County Dublin, Ireland 1 week ago Medical Laboratory Aide 0.50 WTE SCH0652025 Dublin, County Dublin, Ireland 6 days ago Dublin, County Dublin, Ireland 4 days ago In Process Control Laboratory Analyst - APICOM Dublin, County Dublin, Ireland 5 days ago Dublin, County Dublin, Ireland 1 week ago AI Lab - ML and Data Science freeform submission 12-Month Research Assistant in Advanced Digital Skills Dublin, County Dublin, Ireland 1 week ago Dublin, County Dublin, Ireland 2 weeks ago Research Assistant in on Computational Social Science Dublin, County Dublin, Ireland 2 days ago Dublin, County Dublin, Ireland Dublin, County Dublin, Ireland #J-18808-Ljbffr
Overview Electronic Hardware Engineer - Medical Device The purpose of this position is to collaborate with other engineering teams to design and develop hardware to ensure the final product operates correctly. This role involves product design and testing for electro-mechanical controllers and software to ensure performance and safety certification IEC60601-1 is met. The role is with an industry-leading medical device company based in Dublin undergoing a transformation project for a life-saving electromechanical device. Responsibilities Research and develop embedded hardware designs for medical drug delivery combination devices Become a Subject Matter Expert (SME) on systems architecture designs with the ability to present them Test and validation of prototype designs and perform hardware design reviews Work with leading technologies such as LoRa, 5G, and wired interfacing systems Cross-collaborate with different engineering teams Requirements 3 years’ industry experience in electronic design and development Medical device experience is not required but is preferable Experience in C or C++ Knowledge and experience with CAD packages or similar Strong understanding of embedded software development Seniority level Associate Employment type Full-time Job function Engineering, Design, and Project Management Industries Medical Equipment Manufacturing Pharmaceutical Manufacturing Engineering Services #J-18808-Ljbffr
Looking for a Mechanical Engineer to join a Global Device Engineering team who are helping to develop a new complex medical devices. What You’ll Do: Lead engineering activities for new and sustaining products Design electromechanical and plastic components Build and test prototypes Solve engineering challenges and support technical reviews What You’ll Bring: 3+ years’ experience (regulated environment preferred) Strong problem-solving and prototyping skills Seniority level: Associate Employment type: Full-time Job function: Medical Equipment Manufacturing We are an equal opportunities employer and welcome applications from all qualified candidates. #J-18808-Ljbffr
