Are you interested in taking the next step in your career with a global leader in medical devices and healthcare? Are you ready to challenge yourself and lead initiatives in a fast-paced environment? Do you have a background in life sciences? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description Our client in Tipperary are seeking an experienced Senior Engineer to lead initiatives on-site that are primarily focused on their equipment and systems across packaging, sterilization and shipping processes. A minimum of 5 years of engineering experience in a regulated manufacturing environment are required for this senior role. Key Responsibilities Lead engineering initiatives with a strong focus on the full equipment and systems validation lifecycle (IQ/OQ/PQ), across packaging, sterilisation, and shipping processes ensuring alignment with internal procedures and regulatory standards. Evaluate, select, and implement new equipment, technologies, and processes through rigorous research, analysis, and application of engineering best practices. Manage backend operations-including packaging, sterilisation, and shipping-to meet production targets and maintain seamless supply chain performance. Drive automation and digitalisation projects to enhance operational efficiency, reliability, and compliance. Support product and process validation activities, including documentation development and execution of qualification protocols. Collaborate on new product introductions and technology transfers, ensuring smooth integration into existing manufacturing systems. Identify and lead process improvement initiatives using Lean, Six Sigma, or equivalent methodologies to reduce waste and optimise performance. Review and contribute to technical documentation, change controls, reports, and memos to support continuous improvement and knowledge transfer. Provide hands‑on technical leadership and mentorship to junior engineers and technicians, fostering a culture of learning and accountability. Ensure full compliance with GMP, FDA, BSI, EEO regulations and internal quality systems, supporting audits and inspections as required. Actively participate in cross‑functional teams, working closely with Quality, Regulatory Affairs, Operations, and Supply Chain to deliver business‑critical outcomes. Key Requirements Bachelor's degree in Mechanical, Manufacturing, or Biomedical Engineering (Level 8 preferred). Minimum 5 years' experience in a regulated manufacturing environment (MedTech or pharma). Proven experience in at least two or more of the following: Packaging, Sterilisation, Shipping, Automation, Validation, Process Improvement, Product Launches. Strong understanding of GMP, validation protocols, and risk management. Hands‑on experience with equipment troubleshooting, process optimisation, and documentation. Familiarity with technical writing, including protocols, reports, and SOPs. Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid public holidays Location Clonmel, Ireland | onsite #J-18808-Ljbffr
A global leader in biologics is looking for a QC Raw Materials and Compendial Scientist in Dundalk, Ireland. The ideal candidate will have a strong GMP background, experience with compendial and HPLC testing, and excellent technical writing capabilities. Responsibilities include ensuring safe laboratory operations, supporting quality system development, and training personnel. This role offers a competitive compensation package and is on-site. Don't miss this opportunity to advance your career! #J-18808-Ljbffr
A global leader in medical devices is seeking an experienced Senior Engineer in Clonmel, Ireland. The role requires leading engineering initiatives across packaging, sterilisation, and shipping processes. Candidates should have over 5 years of experience in a regulated manufacturing environment and a strong understanding of GMP and validation protocols. The position offers a competitive compensation package, including health insurance and pension contributions, aimed at driving innovation in a fast-paced environment. #J-18808-Ljbffr
Are you interested in taking the next step in your career with a global leader in biologics? Are you a scientist looking to progress your career and support the discovery, development and manufacturing of novel medicines? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description Our client in Dundalk is seeking a QC Raw Materials and Compendial Scientist to be responsible for performing and supporting quality control testing of raw materials and compendial assays critical to biologics manufacturing. Key Responsibilities Ensure safe startup and routine operation of QC Raw Materials and Compendial laboratory functions. Support laboratory setup, equipment installation/qualification, and facility qualification activities. Develop and maintain quality systems (SOPs, documentation, training materials). Perform or support test method development and validation, and routine testing strategies. Author and review technical documents including protocols, validation reports, SOPs, etc. Participate in investigations (OOS/OOL), change controls, CAPAs, and quality events. Monitor laboratory KPIs and manage stock of reagents and consumables. Support internal and external audits and regulatory inspections. Train and mentor QC analysts and other personnel on methods and procedures. Engage with cross-functional teams and clients as needed. Key Requirements GMP laboratory experience 3+ years Experience with pharmacopoeia, monographs (EP, USP, JP) Experience with compendial testing: pH, osmolality, appearance, KF. HPLC experience Technical writing capabilities: with experience on quality event systems such a Trackwise and ability to write deviations, laboratory events, CAPAs, change controls etc. Previous project management experience an advantage but not essential Highly motivated individual required who is a 'go-getter', able to work independently and meet deadlines. Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid holidays Location Dundalk, Ireland | on-site #J-18808-Ljbffr
A leading global medical devices company is seeking a Senior Engineer based in Clonmel, Ireland. The role involves leading engineering initiatives across packaging, sterilisation, and shipping processes. Candidates should have a Bachelor's degree in Mechanical, Manufacturing, or Biomedical Engineering along with a minimum of 5 years in a regulated manufacturing environment. Competitive compensation, pension contributions, and health insurance are part of the attractive package offered. #J-18808-Ljbffr
Are you interested in taking the next step in your career with a global leader in biologics? Are you a scientist looking to progress your career and support the discovery, development and manufacturing of novel medicines? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description Our client in Dundalk is seeking a QC Raw Materials and Compendial Scientist to be responsible for performing and supporting quality control testing of raw materials and compendial assays critical to biologics manufacturing. Key Responsibilities Ensure safe startup and routine operation of QC Raw Materials and Compendial laboratory functions. Support laboratory setup, equipment installation/qualification, and facility qualification activities. Develop and maintain quality systems (SOPs, documentation, training materials). Perform or support test method development and validation, and routine testing strategies. Author and review technical documents including protocols, validation reports, SOPs, etc. Participate in investigations (OOS/OOL), change controls, CAPAs, and quality events. Monitor laboratory KPIs and manage stock of reagents and consumables. Support internal and external audits and regulatory inspections. Train and mentor QC analysts and other personnel on methods and procedures. Engage with cross-functional teams and clients as needed. Key Requirements GMP laboratory experience 3+ years. Experience with pharmacopoeia, monographs (EP, USP, JP). Experience with compendial testing: pH, osmolality, appearance, KF. HPLC experience. Technical writing capabilities with experience on quality event systems such as Trackwise and ability to write deviations, laboratory events, CAPAs, change controls, etc. Previous project management experience an advantage but not essential. Highly motivated individual required who is a 'go-getter', able to work independently and meet deadlines. Competitive and attractive employee compensation package. Pension contributions. Health insurance. Paid holidays. Benefits Competitive and attractive employee compensation package. Pension contributions. Health insurance. Paid holidays. Location Dundalk, Ireland | on-site #J-18808-Ljbffr
Are you interested in taking the next step in your career with a global leader in medical devices and healthcare? Are you ready to challenge yourself and lead initiatives in a fast‑paced environment? Do you have a background in life sciences? You could be the perfect candidate for this opportunity! Don’t hesitate, apply today! Job Description Our client in Tipperary is seeking an experienced Senior Engineer to lead initiatives on‑site that are primarily focused on equipment and systems across packaging, sterilisation and shipping processes. A minimum of 5 years of engineering experience in a regulated manufacturing environment is required for this senior role. Key Responsibilities Lead engineering initiatives with a strong focus on the full equipment and systems validation lifecycle (IQ/OQ/PQ) across packaging, sterilisation and shipping processes, ensuring alignment with internal procedures and regulatory standards. Evaluate, select and implement new equipment, technologies and processes through rigorous research, analysis and application of engineering best practices. Manage backend operations – including packaging, sterilisation and shipping – to meet production targets and maintain seamless supply‑chain performance. Drive automation and digitalisation projects to enhance operational efficiency, reliability and compliance. Support product and process validation activities, including documentation development and execution of qualification protocols. Collaborate on new product introductions and technology transfers, ensuring smooth integration into existing manufacturing systems. Identify and lead process improvement initiatives using Lean, Six‑Sigma or equivalent methodologies to reduce waste and optimise performance. Review and contribute to technical documentation, change controls, reports and memos to support continuous improvement and knowledge transfer. Provide hands‑on technical leadership and mentorship to junior engineers and technicians, fostering a culture of learning and accountability. Ensure full compliance with GMP, FDA, BSI, EEO regulations and internal quality systems, supporting audits and inspections as required. Actively participate in cross‑functional teams, working closely with Quality, Regulatory Affairs, Operations and Supply Chain to deliver business‑critical outcomes. Key Requirements Bachelor’s degree in Mechanical, Manufacturing or Biomedical Engineering (Level 8 preferred). Minimum five years’ experience in a regulated manufacturing environment (MedTech or pharma). Proven experience in at least two or more of the following: Packaging, Sterilisation, Shipping, Automation, Validation, Process Improvement, Product Launches. Strong understanding of GMP, validation protocols and risk management. Hands‑on experience with equipment troubleshooting, process optimisation and documentation. Familiarity with technical writing, including protocols, reports and SOPs. Benefits Competitive and attractive employee compensation package Pension contributions Health insurance Paid public holidays Location Clonmel, Ireland | onsite #J-18808-Ljbffr
A leading global biopharmaceutical company is seeking a QC Raw Materials and Compendial Scientist in Dundalk, Ireland. The successful candidate will be responsible for quality control testing of raw materials and compendial assays critical to biologics manufacturing. Strong experience in GMP laboratories and knowledge of compendial testing methods are essential. This role offers a competitive compensation package, including pension contributions and health insurance, with a focus on professional growth and development. #J-18808-Ljbffr
Have you ever wondered if a career in Sales is for you? Sales Academy Programme Cork Office. Oxford Global Resources, a global Staffing & Professional Services firm with 40 years of experience, is seeking motivated and results-driven individuals to join our team. We have an exclusive and exciting 8-week Sales Academy Training Programme beginning at our Cork office, with the potential of full time Account Management positions being offered, after the initial 8 -weeks. Oxford, as a company, has 35 offices globally, and provides niche professional services in IT, Engineering, Life Sciences and Lab Services to some of the best-known companies across the globe, partnering with brands such as Amazon, Tesla, Anheuser Busch, Johnson & Johnson, Pfizer, Moderna, Whole Foods, and many more. Our Sales Academy Training Programme offers a unique opportunity to learn, grow, and make an immediate impact within our business. We are committed to providing you with comprehensive training in business-to-business sales supporting our Account Managers and Recruiters, and to show the possibilities of how one phone call can potentially become a multi-million dollar partnership. What to Expect: Account Management: You will learn and support our unique Account Management sales process across Oxford's various divisions. You will learn and understand the critical skills clients in the Technology and Life Sciences sectors regularly look for when hiring consultants. You will sell Oxford and our value proposition to critical decision makers within organizations that utilize our services. Hands-On Experience: You will gain practical experience in conducting business-to-business sales. You will learn to network an organization utilizing various sales approaches and technology phone calls, emails, text, Salesforce CRM, and LinkedIn to foster and grow Oxfords relationships within current and new organizations. Mentorship: You will partner with and learn from some of the industry's most talented and passionate sales professionals. Oxford has won numerous awards and accolades over our 40 years ClearlyRateds Best in Staffing Client and Talent, Top Workplaces, ATD Excellence in Practice, and more. You will learn first hand what it takes to be successful in the highly rewarding world of professional services. Qualities We Value: Competitive Fire: We're looking for individuals who thrive on challenges and are motivated to excel in a competitive environment. Strategic Mindset: We deal with some of the biggest and best companies in the world and we look for people who can strategically position Oxford and make us stand out from the crowd. Positive Attitude and Strong Work Ethic: A positive attitude and a strong commitment to hard work are essential for success in our fast-paced setting. Team Player: Our Sales & Recruitment staff, though driven individuals, do their best work as a team and this is key to Oxfords success the last 40 years. Determination: A strong desire to learn and grow within our organization and continue your career in sales. Benefits: Compensation: An hourly rate of pay, plus monetary incentives for achieving targets, as well as weekly Top Performer cash bonuses! Environment: You will work hand-in-hand with a peer group of other motivated and talented future Account Managers. Oxford is distinguished by our amazing culture of winning, integrity, agility, and teamwork. These values are the bedrock of our firm and portrayed by every individual throughout the company. Further, our offices offer modern workspaces, on-site free parking, kitchen, our own gym with personal training classes, and lounge spaces with ping-pong tables, lovely coffee and more! Oxford Cares:You will have the opportunity to get involved with our outreach Programmes which provide involvement in environmental sustainability, community outreach, and diversity and inclusion. These are just some ways Oxford intends to leave our mark in the communities we serve. Opportunity for Promotion and Advancement: Our Sales Academy Programme is a launchpad for future opportunities and career growth within Oxford. This is a 32 hour a week role with potential to convert to full-time after programme completion. Certificate of Completion: Every person who joins us for this 8 - week programme will be awarded a certificate of completion at the end of the course. This will be a fantastic addition to your CV to outline the training you received at a US Multinational Corporate Company who are at the forefront of the Staffing & Recruiting Industry. Don't miss this chance to gain valuable experience and be part of our dynamic team. Apply today to start your journey with Oxford! Skills: Sales Business Business Development Consulting Client Engagement Account Management Benefits: Laptop Performance Bonus Gym
