Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. Why join us? BD is proud to be certified as a Top Employer 2026 in United Kingdom , reflecting our commitment to creating an exceptional working environment BD is proud to be certified as a Top Employer 2026 in Poland , reflecting our commitment to creating an exceptional working environment BD is proud to be certified as a Top Employer 2026 in Spain , reflecting our commitment to creating an exceptional working environment BD is proud to be certified as a Top Employer 2026 in Italy , reflecting our commitment to creating an exceptional working environment BD is proud to be certified as a Top Employer 2026 in Saudi Arabia , reflecting our commitment to creating an exceptional working environment A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. Become a maker of possible with us! Our vision for Integrated Supply Chain at BD The Supply Chain team are responsible to bringing billions of life‑saving medical devices and diagnostics tests, high-tech instruments and equipment to customers and patients all over the world. Our aim is deliver these products at an affordable cost and of the highest quality. About The Role Contract Manufacturing Director you will be responsible for the strategic and operational leadership of all outsourced pharmaceutical systems manufacturing activities. The role ensures that Contract Manufacturing Organizations (CMOs) deliver products safely, compliantly, on time, and at the right cost and quality. you will act as the primary interface between the company and CMOs, driving performance excellence, ensuring regulatory compliance, and optimizing the external supply network. Main Responsibilities Will Include CMO Governance & Performance Management Lead the relationship with assigned CMOs, ensuring strong operational performance and continuous improvement. Establish and oversee governance structures. Monitor key metrics. Lead issue escalation, resolution pathways, and structured problem‑solving with CMO partners. External Manufacturing Strategy Develop and execute the external manufacturing strategy for assigned product portfolio. Assess capabilities, risks, and opportunities across the CMO landscape. Contribute to make/buy decisions, outsourcing strategies, and network optimization initiatives. Support business case development for transferring products to new CMOs or scaling capacity. Operational Excellence & Cost Management Drive productivity programs and cost‑reduction initiatives across the external network. Ensure robust demand planning, capacity planning, and inventory strategies with CMOs. Review and challenge CMO proposals for cost adjustments, change controls, and capital needs. Negotiate commercial and operational terms in partnership with Procurement. Quality & Compliance Ensure CMOs operate in full compliance with cGMP, ICH, FDA, EMA, and global regulatory standards. Partner with Quality Assurance on audits, inspection readiness, and remediation plans. Oversee change controls, deviation investigations, CAPAs, and risk assessments related to outsourced manufacturing. Support regulatory submissions (CMC sections, responses to HA queries, product variations). Technology Transfer & Lifecycle Management Lead or support technology transfer activities to and from CMOs. Coordinate technical teams for process validation, scale‑up, and launch readiness. Drive lifecycle management activities, including formulation changes, process improvements, and cost optimization projects. Ensure robust knowledge transfer and documentation standards during transfers. Cross‑Functional Leadership Partner with Supply Chain, Quality, Regulatory, Procurement, R&D, Finance, and Technical Operations to ensure end‑to‑end performance. Provide leadership to multidisciplinary project teams involving internal and external stakeholders. Act as the internal subject‑matter expert for external manufacturing strategy and performance. About You We are looking for an accomplished supply chain leader with a strong track record in managing Contract Manufacturing Organizations (CMOs) across diverse regions and pharmaceutical technologies. The ideal candidate will bring: A minimum of 10 years of experience in the pharmaceutical industry. At least 5 years of direct experience in external/contract manufacturing. Proven leadership in managing CMOs across multiple geographies and technologies, including (but not limited to) sterile manufacturing, oral solid dose, biologics, active pharmaceutical ingredients (API), and packaging. To be successful in this role, you should be able to demonstrate: Strategic Vision: Ability to shape external manufacturing networks and anticipate risks. Technical Depth: Solid grasp of manufacturing technologies, quality, and regulatory standards. Influence & Negotiation: Skilled in leading without authority and managing external partners. Analytical Thinking: Strong problem‑solving and data‑driven decision‑making. Operational Rigor: Proven track record in planning, execution, and performance management. Collaborative Leadership: Effective in matrixed, cross‑functional environments. Business Insight: Understanding of cost drivers, contracts, and financial levers. Click on apply if this sounds like you! At BD, we prioritize on‑site collaboration because we believe it fosters creativity, innovation, and effective problem‑solving, which are essential in the fast‑paced healthcare industry. For most roles, we require a minimum of 4 days of in‑office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work‑life balance. Remote or field‑based positions will have different workplace arrangements which will be indicated in the job posting. Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics. To learn more about BD visit: https://bd.com/careers Required Skills Primary Work Location GBR Swindon - Dorcan Additional Locations IRL Dun Laoghaire - Pottery Road Work Shift At BD, we are strongly committed to investing in our associates—their well‑being and development, and in providing rewards and recognition opportunities that promote a performance‑based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location. Salary Range Information £101,700.00 - £155,100.00 GBP Annual #J-18808-Ljbffr
A leading global medical technology company is seeking a Contract Manufacturing Director in Ireland to strategically lead outsourced pharmaceutical systems manufacturing. This role demands strong leadership and management of Contract Manufacturing Organizations (CMOs) to ensure compliance, quality, and timely delivery. The ideal candidate should have over 10 years of experience, focusing on external manufacturing in the pharmaceutical industry. This position promotes on-site collaboration to foster creativity and innovation. #J-18808-Ljbffr
Summary The Software Test Engineer will be responsible for testing of medical device software on our new product lines and supporting existing products. This role involves developing test systems and procedures to ensure that the software meets all requirements and works correctly in all situations. The successful candidate will have experience in testing embedded software, ideally within the medical devices industry. They should also be familiar with IEC 62304, IEC 80002-1 and IEC 80002-2 standards. Knowledge of regulatory requirements such as MDSAP would be beneficial. About The Role As a Senior Software Test Engineer, you will play a key role in ensuring the quality and reliability of Software for medical devices. You will work within an agile team environment or independently, driving Software Test Automation and TA frameworks, and supporting both development and sustaining activities. This role requires strong technical expertise, attention to detail, and a proactive approach to continuous improvement. Main Responsibilities Contribute to an agile team or work independently on medical device testing. Drive Software Test Automation and its Frameworks to increase TA coverage. Take ownership of assigned tasks and deliver on schedule. Provide timely feedback on test estimates and progress to the Test Lead. Understand and interpret requirements for testing. Write, review, and execute test cases; capture findings in a structured manner. Define, generate, and review test documentation (Test Plans, Test Reports). Support troubleshooting, characterization, and validation for prototypes and subsystems. Assist with sustaining activities and process improvements. Engage in continuous improvement of test processes and practices. Develop test systems and procedures to ensure compliance and functionality. Investigate discrepancies between expected and actual behavior. Liaise with developers to retest fixed bugs and review documentation. Support SDLC/STLC process improvements and maintain test scripts. Qualifications & Experience Education: Minimum Level 8 degree in Computer Science or related discipline. Experience 6+ years in software testing (manual and automation). Strong experience in Test Automation and TA frameworks. Experience with embedded software testing, preferably in medical devices. Technical Skills SQL, API Testing, Embedded Software. Python, Robot Framework, BDD, KDT (advantageous). Familiarity with IEC 62304, IEC 80002-1, IEC 80002-2 standards. Other Skills Excellent communication and documentation skills. Strong analytical and problem-solving abilities. Ability to work independently and manage time effectively. Good understanding of hardware and OS internals. Knowledge of software configuration management principles. Additional Flexibility for occasional extended hours/weekends to meet critical deadlines. Desired Attributes Proactive mindset with attention to detail. Strong collaboration skills within cross-functional teams. Commitment to continuous improvement and quality assurance. Click on apply if this sounds like you! Primary Work Location IRL Limerick - Castletroy Work Shift We require a minimum of 4 days of in-office presence per week. Remote or field-based positions will have different workplace arrangements indicated in the job posting. Equal Opportunity Employer Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Salary Range €54,800.00 - €83,600.00 EUR Annual #J-18808-Ljbffr
A leading medical device company in Limerick is seeking a Senior Software Test Engineer responsible for testing medical device software and driving test automation. The ideal candidate has at least 6 years of experience in software testing, particularly in embedded systems. Strong technical skills in SQL, Python, and testing frameworks are essential. The role requires working in an agile environment, focusing on improving quality and compliance of software products. A comprehensive benefits package and competitive salary range of €54,800.00 - €83,600.00 EUR annually is offered. #J-18808-Ljbffr
