Oxford Global Resources is seeking a Maintenance Technician in Clonmel, Ireland. The role involves maintaining, troubleshooting, and improving automated manufacturing equipment within the medical device sector. Key responsibilities include conducting maintenance on electrical and mechanical systems and ensuring compliance with safety standards and GMP. Candidates should possess mechanical maintenance skills, experience in medical device manufacturing, and knowledge of PLCs. This position is on-site and operates on a shift-based schedule, with a potential for permanency after a six-month contract. #J-18808-Ljbffr
Senior Mechanical Engineer (Contract – Medical Power Electronics) Contract Duration: 3–6 months Location: Onsite (Cork-Office based) Start Date: ASAP Role Overview Our Client is seeking a highly experienced Senior Mechanical Engineering Contractor to support the development and industrialization of high-voltage power supply assemblies used in regulated applications. Experience with medical-grade power electronic modules to IEC60601 would be a bonus but not essential. This role requires an engineer who can hit the ground running, operate with minimal day‑to‑day input, and take ownership of mechanical design activities while aligning with an existing on‑site Senior Mechanical Engineer. The successful candidate will bring deep, hands‑on experience in tooling, tolerance analysis, and PCB‑to‑enclosure integration in safety‑critical electronic systems. Experience in plastics and soft tooling is a must. Key Responsibilities Mechanical Design for Medical Power Electronics Design and develop mechanical solutions for medical power electronic modules, including: Structural frames, metal panels and enclosures PCB support and retention features Patient and operator safety, electrical isolation and physical robustness Manufacturability for low‑to‑medium‑volume medical builds Soft Tooling (Medical Device Context) Lead soft tooling efforts for: Large plastic frames (A4 sized) used in medical electronic modules Metal panels and covers used in power electronics assemblies Work directly with tooling vendors to: Enable rapid iteration and controlled changes Resolve fit, warp, cosmetic, and tolerance‑related issues Ensure tooling choices are appropriate for medical NPI or pilot production environments. Tolerance & Mechanical Stack‑Up Analysis Perform and document mechanical tolerance stack‑ups for: Modular power electronics architectures Identify mechanical risks impacting connector mating and alignment Enclosure stack‑up and fastener preload PCB‑to‑enclosure mounting points Connector alignment (HV, LV, signal) Enclosure closure interfaces (covers, frames, seals) Isolation barriers and insulating features External interfaces (mounting feet, chassis rails, cable exits) Provide clear, defensible analyses suitable for design reviews and regulated documentation. PCB & Enclosure Integration (High Voltage, Medical Safety) Integrate A4‑sized PCBs into mechanical housings with focus on: High‑voltage insulation and spacing Mechanical protection of HV components Isolation barriers and insulating features Number and location of mounting points Fixed vs floating mounts (slots vs round holes) Over‑constraint risk (especially with large A4 PCBs) Ability to absorb tolerance and enclosure distortion Long edge support vs point support Local stiffening needed near connectors or heavy components Need for secondary supports (insulators, pillars, ribs) PCB warp tolerance considered in stack Enclosure flatness vs PCB flatness assumptions Interaction between fastener pull‑down and PCB bending Design enclosures compatible with: Thermal management needs of power electronics Service access and controlled replacement Medical safety expectations (finger‑safe, shielding, robustness), detail drawings STEP and neutral file exports CAD, Drawings & Design Control Organize and rationalize existing CAD data into a clean, controlled structure, including: Assembly models Ensure drawings: Clearly convey design intent Align with medical device design control expectations Operate autonomously while aligning with the on‑site Senior Mechanical Engineer on: Risk trade‑offs and escalation items Collaborate effectively with: Electrical engineering Manufacturing and suppliers Quality and regulatory stakeholders as needed Deliver designs and documentation within aggressive project timelines. Required Qualifications & Experience 6+ years of mechanical engineering experience, preferably in: Proven hands‑on experience with: Soft tooling for plastic frames and housings Soft tooling for metal panels or enclosures Strong competency in mechanical tolerance analysis for complex electronic assemblies. Extensive experience integrating large PCBs into enclosures for high‑voltage power applications. Proficient in professional 3D CAD tools (specifically SolidWorks). Ability to work with minimal supervision and make sound technical decisions in alignment with the on‑site Sr. Mech Eng. Power electronics Safety‑critical electronic systems Medical devices (Nice to have) Familiarity with medical device safety standards impacting mechanical design (e.g., IEC 60601 concepts such as spacing, accessibility, and enclosure integrity). Experience supporting medical NPI, pilot builds, or design transfer activities. Prior contract or consultancy experience in regulated environments. Personal Attributes High degree of English competency with excellent spoken and written English. Proven ability to communicate complex mechanical concepts clearly and concisely to electronic, manufacturing and quality stakeholders. Capable of producing clear, unambiguous technical documentation (e.g., drawings, tolerance analyses, design notes, etc.). Highly self‑directed and execution‑focused. Detail‑oriented with strong appreciation for manufacturing and safety constraints. Clear communicator capable of concise documentation suitable for a regulated product environment. Duration: 6 months (potential move to permanent) Work Model: Primarily onsite to enable effective collaboration (hybrid considered) #J-18808-Ljbffr
Oxford Global Resources is looking for a skilled Senior Mechanical Engineer in Cork for a contract role focused on medical power electronics. The engineer will design mechanical solutions, lead tooling efforts, and conduct tolerance analyses. Candidates should have over 6 years of experience, including in regulated environments, and proficiency in SolidWorks is essential. The position offers the potential for a permanent role and emphasizes effective communication within a hybrid work environment. #J-18808-Ljbffr
Technical Recruiter (Life Sciences) Cork Who We Are Since 1984, Oxford Global Resources has focused on building trust with each interaction. Were proud to create long-lasting relationships with the brightest minds in industry, while continuing to identify and drive initiatives that advance our clients business. Oxford is known for our unmatched ability to deliver The Right Talent. Right Now. As a leading Staffing and Consulting company with offices across North America and Europe, we focus on proactively building a network of highly skilled professionals across 4 key disciplines - Life Sciences, IT, Lab Services & Engineering to assist our most valued asset, Our Clients, in achieving their goals. Position Summary As a Life Sciences Recruiter, you will be tasked with pro-actively recruiting top talent, building relationships with them, and assigning them to critical, niche, highly-skilled roles in some of the biggest companies in the world. You will be the main point of contact for our freelance consultants from the time they sign on with us, through their assignment with our clients, ideally continuing that relationship and support their career goals with additional consulting positions. If you are an energetic, self-motivated, networker, youll develop an extremely rewarding recruiting career both professionally and financially. What We Offer Competitive, combined package of base salary, fully uncapped commission, and various other bonus opportunities. A Dynamic Career Opportunity with travel opportunities to client sites across Europe, and to our own offices in Amsterdam, Barcelona, Dusseldorf Antwerp and Zug. Opportunity to sell unique, highly-specialized staffing solutions and to become a trusted partner to some of the largest and best companies in the world. Full Healthcare, Vision and Dental plans On-site gym and on-site parking at our Penrose Offices in Cork City. A collaborative work environment where you can thrive as an individual, and know that you are supported every step of the way Team-building activities and social events in and outside of the office Ongoing training and career advancement Opportunity for high-performers to qualify for Presidents Club Responsibilities Pro-actively recruit technical consultants in the Life Sciences sector across Europe and further afield. Establish rapport and build relationships with technical consultants to assess their needs and wants, the skills they maintain, and overall fit for our clients. Respond to open job opportunities by vetting your consultants and presenting qualified candidates to clients. Negotiate consultant conditions, rates and close offers. Prepare consultants for interviews. Manage consultants while on assignment for Oxford. Input consultant information and all communication notes into the database. Qualifications Excellent communication skills, both verbal and written, in English is a must have fluency in another major European language is a plus. Self-motivated, high-energy personality. Competitive, goal-oriented mindset. Some Recruitment experience (1-2 years) in an agency or in-house environment is advantageous. Ideally some knowledge of Systems & Tools such as MS Office, LinkedIn (Recruiter), Salesforce CRM, etc. Note: This role is based 5 days per week on-site initially at our Cork Office. There are remote opportunities in time. Skills: Recruitment Sales Life Sciences Benefits: Gym Pension Health Insurance On-site Parking Uncapped Commission Laptop TPBN1_IJ
Are you interested in taking the next step in your career with a global leader in the life sciences industry? Are you ready to challenge yourself in a fast-paced and highly regulated environment? Are you an experienced IT Validation Engineer with a background in GxP? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description Our client in Ireland are seeking experienced IT Compliance & Validation Engineers (CSV) to join their team and support validation activities for applications, systems and digital solutions. You will apply IT, quality and regulatory compliance expertise to assess system requirements against validation and assurance activities using risk-based CSA principles. Key Responsibilities Ensure compliance with applicable GxP regulations, corporate quality policies, and divisional procedures, including data integrity and electronic records requirements Develop and maintain risk-based validation and CSA strategies for medium to large systems Define validation and assurance approaches for AI-enabled systems used in regulated activities (e.g., quality, manufacturing, laboratory, supply chain, clinical, or safety) Develop, review, and approve validation documentation, including Validation Plans, CSA strategies, risk assessments, test plans, protocols, summary reports, and AI impact assessments, in accordance with SLC and quality system requirements Support and review automated testing and assurance activities, ensuring testing effort is focused on critical system functionality consistent with CSA principles Identify, escalate, and resolve compliance issues that may introduce regulatory, patient safety, product quality, or data integrity risk Key Requirements Bachelor's Degree with experience in a regulated life sciences IT or quality systems environment Demonstrated experience with GxP computer system validation (CSV) and Computer Software Assurance (CSA) in pharmaceutical, biotech, or medical device environments. Experience supporting or validating AI-enabled, automated, or data-driven systems used in GxP processes, with understanding of data integrity, audit trails, security, and lifecycle controls. Strong understanding of global life sciences regulations and guidance (e.g., 21 CFR Part 11, EU GMP Annex 11, FDA CSA guidance). Strong written and verbal communication skills, with proven ability to collaborate with IT, Quality, Regulatory, and business stakeholders in regulated environments. Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid public holidays Location: Cork/Dublin, Ireland | remote #J-18808-Ljbffr
Oxford Global Resources is seeking an IT Compliance & Validation Engineer to join a team in Cork. The role involves ensuring compliance with GxP regulations and developing validation strategies for AI-enabled systems. Candidates should have a Bachelor's Degree and experience in GxP computer system validation. Benefits include competitive compensation, health insurance, and pension contributions. The position offers a blend of onsite and remote work. #J-18808-Ljbffr
Business Development Executive, Life Sciences Industry – Dublin, Ireland (Hybrid) Who We Are Since 1984, Oxford Global Resources has delivered high-impact consulting, contract staffing, and project-based solutions to organisations globally. We specialise in workforce mobilisation, digital transformation, and modern enterprise solutions, with a strong presence across the Life Sciences sector. Position Summary As a Business Development Executive within our Life Sciences division, you will take ownership of developing new client relationships and expanding existing accounts across the Leinster region. You will partner with senior stakeholders to understand strategic priorities, identify capability gaps, and position Oxford’s consulting solutions and Contract Staffing capabilities to drive measurable business outcomes. You will be supported by a structured onboarding programme and ongoing enablement, allowing you to quickly build market expertise and maximise your earning potential through our uncapped commission structure. This role suits a commercially driven, relationship-focused professional who thrives in a target-driven environment and enjoys building long-term client partnerships. What We Offer Uncapped earning potential with a competitive base salary and commission structure Opportunity to sell unique, highly-specialised consulting and contract staffing solutions and to become a trusted partner to some of the largest and best Life Sciences companies in the world. Health Insurance (Level Health), Vision and Dental & Company Pension Contribution Team-building activities and social events in and outside of the office On-going training and career advancement Opportunity for high-performers to qualify for President’s Club The Job Proactively identify, engage, and convert new business opportunities while growing existing client relationships across the Life Sciences sector. Manage the full sales cycle from prospecting through to negotiation and close Build and maintain a strong pipeline to consistently meet or exceed targets Develop and maintain client relationships and ensure Oxford is positioned as a preferred services partner by gathering organisational information such as consultant usage trends; exchanging market data; assisting Clients in defining their needs and advising on methods to meet those needs. Develop sales opportunities by identifying key decision makers at Clients that utilise technical consultant services. Complete Sales and Engagement reporting and operate within our CRM system. Ensure the timely completion of Consulting Services Agreements and credit checks. Complete special projects, lead office projects and other responsibilities as assigned. Critical Tasks Consistently achieve or exceed individual sales targets and KPIs Actively contribute to team success through collaboration and knowledge sharing Represent Oxford in the market through client meetings, industry events, and networking activities You Proven experience in B2B sales, ideally within consulting or staffing in the Life Sciences industry Track record of meeting or exceeding sales targets Strong communication and stakeholder management skills, with the ability to engage senior decision-makers Highly self-motivated, results-driven, and comfortable operating in a fast-paced environment Strong organisational skills and ability to manage multiple priorities Education Bachelor’s Degree (preferred) Location: Home-based role with regular travel across the Leinster region for client meetings and industry events. #J-18808-Ljbffr
Oxford Global Resources is seeking a Business Development Executive to enhance client relationships and expand accounts in the Life Sciences sector across Dublin, Ireland. The role involves identifying new business opportunities, managing the sales cycle, and partnering with clients to meet their needs. The ideal candidate will possess proven B2B sales experience, strong communication skills, and a Bachelor’s Degree is preferred. Competitive salary with uncapped commission structure and various health benefits offered. #J-18808-Ljbffr
Oxford Global Resources in Galway is looking for a Lab Manager to lead a medical device prototyping lab. This position involves managing a team of engineers and technicians, overseeing lab operations, and coordinating multiple prototyping projects. The ideal candidate will have a background in engineering or medical devices, strong technical and project management skills, and the ability to effectively communicate with customers and stakeholders. The role offers a competitive compensation package, including health insurance and pension contributions. #J-18808-Ljbffr
Job Description A global medical device manufacturer in Galway is seeking a Lab Manager to lead a medical device prototyping lab, managing a small team while coordinating projects, customers, and global engineering teams. This role blends people leadership, lab operations, technical oversight, and customer engagement in a fast‑paced environment. Key Responsibilities Lead and manage a team of engineers and technicians (~ 5 - 10 people) Oversee daily operation of the prototyping lab, managing lab resources (e.g. equipment and maintenance, materials and inventory) and ensuring compliance with relevant quality and regulatory standards Plan and coordinate multiple prototyping projects simultaneously Allocate resources effectively across projects Manage timelines, priorities, and deliverables Support rapid turnaround of prototype builds Coordinate with engineering and prototyping teams in the US and India Act as a key interface for customers on prototyping projects Understand customer requirements and translate them into lab deliverables Communicate project status, timelines, and technical updates Support or contribute to quote development for prototype work Drive improvements in lab efficiency, turnaround time, and processes Key Requirements Background in engineering, prototyping, or medical devices preferred Strong technical understanding with ability to guide engineering work Experience managing lab operations, equipment, and resources Proven ability to manage multiple projects and priorities Experience with resource planning and allocation Experience working with cross‑functional and/or global teams Ability to understand customer needs and communicate solutions clearly Excellent verbal and written communication skills Ability to adapt communication style to different audiences Strong stakeholder management Comfortable working at pace and making decisions with changing priorities Exposure to quoting, costing, or commercial decision‑making is advantageous Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid holidays Location: Galway | Ireland #J-18808-Ljbffr
