A global life sciences consultancy is seeking a Senior Director – Strategic Operations to lead the growth of their UK and Ireland presence. This hybrid role entails significant P&L accountability and strategic leadership in client engagement and operational excellence. The ideal candidate will possess a strong engineering background and proven leadership in life sciences. This position offers competitive compensation and the opportunity to shape significant strategies within a dynamic team. #J-18808-Ljbffr
Job Title: Senior Director – Strategic Operations (UK & Ireland) Location: UK (Hybrid) with travel to Ireland Reports To: Regional or Global Leadership Company Overview We are a global life sciences consultancy delivering engineering, technical, and strategic solutions to leading pharmaceutical, biotech, and healthcare organizations. We are expanding our presence in the UK and Ireland and building a new regional team to strengthen client engagement and deliver world-class engineering services. Role Overview We are seeking a Senior Director of Strategic Operations to lead the build-out of our UK and Ireland region. This is a highly visible, hands‑on leadership role with full P&L accountability , overseeing operations, corporate development, client engagement, and technical excellence. The ideal candidate will have a strong engineering background in pharma or life sciences and a proven track record in operational leadership and strategic growth initiatives. This is a hybrid role , based in the UK, with regular travel to Ireland. Key Responsibilities Strategic Leadership & Corporate Development Lead the launch and scale of the UK and Ireland regional operations for the consultancy. Develop and execute strategies for client acquisition, business growth, and market positioning . Drive corporate development initiatives, including partnerships, alliances, and strategic acquisitions. P&L & Operational Accountability Own the P&L for the region, delivering sustainable revenue growth and profitability. Oversee all operational functions, including project delivery, resource management, and process optimization. Establish KPIs and operational dashboards to monitor performance, quality, and efficiency. Client Engagement & Technical Oversight Serve as the senior client engagement leader for engineering services, building long‑term partnerships. Provide technical oversight , ensuring projects are delivered to the highest standards of quality and compliance. Guide teams on complex technical and operational challenges, leveraging your engineering expertise. Team Leadership & Culture Build, mentor, and inspire a high‑performing regional team , fostering a culture of excellence, collaboration, and innovation. Promote knowledge sharing and operational best practices across the global consultancy. Qualifications & Experience Proven leadership experience in life sciences, pharmaceuticals, or related engineering services. Strong engineering background or qualification (chemical, process, mechanical, or pharmaceutical engineering preferred). Demonstrated P&L management and operational leadership experience in multi‑site or regional operations. Experience in corporate development, business growth, or strategic initiatives . Deep understanding of engineering service delivery and client engagement in the life sciences sector. Strong interpersonal, communication, and influencing skills, with experience managing cross‑functional teams . Willingness to travel regularly to Ireland and work in a hybrid environment . Why Join Us Lead the launch of a new regional operation within a growing global life sciences consultancy. Shape strategy and operations at a high‑impact leadership level . Work with a dynamic, entrepreneurial team delivering innovative engineering solutions. Competitive compensation with performance incentives and global career opportunities. #J-18808-Ljbffr
A leading biotech company in Galway is seeking a Principal Scientist to guide the scientific strategy and hands-on execution for novel gene therapies. You will manage programs from discovery through preclinical development, ensuring collaboration across teams and adherence to safety standards. Ideal candidates should have a PhD in life sciences and significant experience in biotech, particularly in therapeutic progression and assay design. The role offers a competitive salary and a key position in a high growth area. #J-18808-Ljbffr
I'm working with an exciting biotech that are looking for a Principal Scientist to lead their scientific direction and hands‑on lab execution for novel exosome‑delivered gene therapies. Your role will be to drive programs from discovery into preclinical development and IND/CTA enabling stages. Work cross‑functionally with internal teams and external partners to advance multiple therapeutic candidates. Responsibilities You will own the scientific strategy and experimental leadership across exosome/gene therapy programs Design and deliver preclinical studies focused on delivery, efficacy, safety, and MoA Develop and validate molecular and cellular potency/identity assays Lead cross‑functional project planning with CMC, translational and regulatory groups Manage collaborations with CRO/academia/industry partners Guide IP‑relevant innovation and scientific documentation Mentor R&D team members and promote lab excellence and compliance Ensure data integrity, SOP adherence, equipment stewardship and safety standards Required Experience PhD in life sciences discipline (molecular/cell biology, gene therapy, immunology etc.) 5–7+ years post PhD experience in biotech or advanced biologics Proven ability to progress therapeutics through discovery to IND enabling work Experience with exosomes/extracellular vesicles or strong motivation to develop expertise Hands‑on analytical assay design and interpretation (e.g., qPCR, flow, ELISA, Western) Familiarity with upstream/downstream process development and scale‑up Understanding of GLP/GMP alignment and documentation for regulatory submissions Skilled in cross‑functional leadership and navigating fast‑moving biotech settings Preferred Respiratory or oncology models Experience supporting IND/CTA or IMPD enabling studies Personal Qualities Hands on, proactive scientific leadership Strong organisation, analytical thinking, and attention to detail Resilient, collaborative and motivated by translational impact What’s Offered Lead cutting edge programs in gene delivery and regenerative medicine Visible role in a high growth biotech with major unmet need focus Competitive salary and performance‑linked compensation Seniority Level Associate Employment Type Full‑time Job Function Research, Analyst, and Information Technology Industries Staffing and Recruiting Location: Galway, County Galway, Ireland #J-18808-Ljbffr
A leading medical device company in Galway, Ireland, is seeking a Senior Research and Development Engineer to innovate and design medical devices. The role requires an honoured degree in Mechanical or Biomedical Engineering and 4+ years of experience in medical device design. Proficiency in SolidWorks is essential, along with strong mechanical engineering skills and a collaborative spirit. The company offers a full-time position in a dynamic and supportive environment. #J-18808-Ljbffr
Senior Research And Development Engineer Join a leading medical device company in Galway, Ireland, as an Senior R&D Engineer. Use your mechanical engineering and CAD skills to design innovative medical devices in a dynamic, collaborative environment. Key Responsibilities Develop device concepts to meet performance goals. Build and test prototypes; analyse data for solutions. Create drawings using SolidWorks. Select materials and assembly methods. Collaborate with cross-functional teams for system integration. Work with vendors to meet project goals. Write protocols and reports; document designs. Ensure ISO 13485 and QMS compliance. Qualifications & Experience Honours degree in Mechanical or Biomedical Engineering or equivalent. 4+ years in medical device design, prototyping, and testing. Proficient in SolidWorks (Autodesk Fusion a plus). Knowledge of ISO 13485 and QMS. Experience in material selection and design validation. Skills & Behaviours Strong mechanical engineering and design skills. Excellent problem-solving and initiative. Strong communication and presentation skills. Team player with multitasking ability. Interest in industry trends and technologies. Seniority level Mid-Senior level Employment type Full-time Job function Medical Equipment Manufacturing #J-18808-Ljbffr
Recruitment Consultant specializing in Commercial & R&D roles within Medical Devices at Barrington James Manufacturing Engineer (Full-Time Onsite) Our client is looking for an innovative and driven Manufacturing Engineer to elevate production operations and support the launch of high-quality, industry-leading products. This role is ideal for someone who thrives in a hands‑on environment, enjoys solving complex challenges, and is passionate about building efficient, scalable manufacturing systems. What You’ll Do Develop, refine, and standardize manufacturing processes to boost efficiency, quality, and throughput. Apply DFM/DFMA principles to ensure robust manufacturability of new and existing products. Partner closely with R&D, Production, and Quality teams to support seamless product development and launch. Drive compliance with ISO 13485, ISO 14001, GMP requirements, and regulatory standards. Analyze production costs, cycle times, and material flow to uncover opportunities for savings and waste reduction. Develop efficient production layouts that support continuous improvement and lean practices. Enhance quality control methods and ensure alignment with industry regulations and best practices. Support FMEA activities, root‑cause analysis, and corrective action initiatives. What You Bring Bachelor’s degree in Industrial, Mechanical, or Manufacturing Engineering Strong experience with CAD/CAM, robotics, automation integration, and manufacturing best practices Knowledge of FMEA, New Product Introduction (NPI), and validation processes (IQ/OQ/PQ) Demonstrated ability to troubleshoot production issues and improve complex systems Excellent written and verbal communication skills Previous experience in a manufacturing or engineering environment If this is of interest, please apply or send a copy of your resume to kpiper@barringtonjames.com Seniority level Associate Employment type Full‑time Job function Medical Equipment Manufacturing Location: Longford, County Longford, Ireland #J-18808-Ljbffr
A leading recruitment firm is seeking a Manufacturing Engineer to enhance production operations in Longford, Ireland. The ideal candidate will have a Bachelor's degree in Engineering and experience in CAD/CAM and automation. Responsibilities include developing manufacturing processes and driving compliance with industry standards. This full-time role offers the opportunity to work on innovative projects in a hands-on environment. #J-18808-Ljbffr
Direct message the job poster from Barrington James Our client, who are operating in the Dublin, are currently recruiting a Quality consultant in the Medical Device space. The company maintains a culture of integrity and compliance, ensuring every product meets global regulatory expectations and exceeds industry quality benchmarks. This is an excellent opportunity to join a growing, international team and contribute to a strong culture of quality and continuous improvement. Key Responsibilities Maintain and continuously improve the QMS in alignment with ISO 13485, MDR & ISO 14971 Lead internal audits and manage audit schedules. Oversee in-process and final inspections, test methods, and release processes. Manage quality documentation for technical files and regulatory submissions. Ensure suppliers meet ISO 13485, GMP, and regulatory expectations. How to apply If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. Applications will be handled in confidence and reviewed on a rolling basis. Seniority level Mid-Senior level Employment type Contract Job functionh3> Quality Assurance Industries Staffing and Recruiting Referrals increase your chances of interviewing at Barrington James by 2x Location: Dublin, County Dublin, Ireland #J-18808-Ljbffr
A leading consulting firm in Dublin is seeking a Quality Consultant to improve the Quality Management System and ensure compliance with ISO standards. This mid-senior level role includes leading audits, overseeing inspections, and managing quality documentation. Join an international team committed to quality and continuous improvement. This contract position offers a unique opportunity to contribute to a robust quality culture. #J-18808-Ljbffr
