A leading life sciences company located in Carrigtwohill, Ireland is seeking a skilled individual in biochemistry or biology to join their R&D team. The role focuses on developing innovative technologies and advancing existing products while collaborating with engineering, marketing, and quality teams. Candidates should have a PhD or Masters in a relevant field, 2+ years of lab experience, and strong problem-solving and communication skills. This position offers opportunities to lead projects and present findings to stakeholders. #J-18808-Ljbffr
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Role The DxRM Account Manager will serve as a strategic partner to customers, focusing on all customers of DxRM products with special focus on Industrial, Testing, Academia and Pharma. They will deliver tailored solutions that support their workflows, ensure supply continuity, and drive operational excellence. A core focus of this field-based role will be expanding the company's footprint within these accounts by identifying unmet needs, increasing market share and seeding new opportunities into customer’s R&D or similar functions in collaboration with DxRM Specialists. The person in this role will be responsible for an assigned territory covering “Assigned Accounts” within a specific geography, achieving sales and gross profit goals of the DxRM portfolio within this geography. Duties Meet or exceed sales targets. Provide detailed and accurate forecasts at scheduled intervals. Partner closely with customers to understand their production processes, pain points, and quality requirements, and providing solutions that enhance efficiency and compliance. Leverage data and customer insights to develop account-specific growth strategies aimed at increasing wallet share and long-term loyalty. Identify opportunities to expand product and service utilization within existing accounts, driving deeper integration of Merck’s portfolio across customer operations. Work to understand the customer’s applications and pain points, share these insights with DxRM R&D and Product Management to ensure strong innovation pipeline. Utilize Salesforce CRM and digital analytics platforms to track customer engagement, forecast demand, and identify cross‑selling opportunities based on usage patterns and workflow gaps. Monitor and understand competitors’ market and product positions. Participate in trade shows as needed. Act as a technical consultant to guide customers in selecting the right DxRM product for their needs. Provide commercial and technical support on DxRM products. Manage all customer inquiries, plant audits, and contract negotiations. Comfortable working in a highly matrixed organization. Who You Are Bachelor’s degree in a scientific/technical field (Biology, Immunology, Molecular Biology, Biochemistry) or Business; advanced degree a plus. (MBA highly desirable). 5+ years of field sales with DxRM / Pharma / IVD / Industrial customers. Demonstrated experience working across either A. The full Industrial product development and manufacturing value chain, B. The Clinical Testing Development chain or C. Pharmaceutical Product Development and Manufacturing chain. Broad-based knowledge of basic scientific procedures, testing methods, and equipment coupled with the ability to diagnose customer needs and provide product solutions. Evidence of disciplined CRM usage and successful navigation of RFP’s, tenders, Supply Agreements and Quality Agreements (SAs and QAAs). Proven track record: highly accurate forecasts (target ±5%), consistent quota delivery, above‑market growth, and 4–5x quota pipeline generation. Positive Price realization within guidance and demonstrated ability to drive exceptional price reductions supported by strong business cases. Fluent in English, written and oral communication. Excellent organization and time management. Business acumen to negotiate long‑term supply agreements. Highly goal‑oriented and self‑motivated, capable of working with minimum direction. Self‑starter, proactive individual with excellent interpersonal and communication skills. Ability to be autonomous and to work in a multicultural environment. Position requires travel to visit customers within the assigned territory and the ability to successfully drive business through face‑to‑face and virtual activities. Ability to be in the field for face‑to‑face customer meetings 4 days a week. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life! #J-18808-Ljbffr
Your Role We are looking for a dynamic, forward-thinking individual with a background in biochemistry / Biology to join our multidisciplinary R&D team responsible for developing new technologies, products, applications and solutions for our existing products. This person will also be working closely with our operations, product management and quality team supporting product line advancement, product changes and customer complaint resolution. Support Existing Product Line Longevity: collaborate closely with operations, engineering and quality teams to ensure the ongoing success and reliability of current products, addressing customer complaints and implementing product changes and projects as necessary. Participate in strategic planning for the product portfolio and identify new areas for future development in life science. Leverage specialized knowledge and analytical skills to solve complex problems. Engage with engineering, marketing personnel and other scientists, as well as with external collaborators and customers. Provide project management and portfolio expertise leadership on cross functional products to support strategy execution of the portfolio. Develop new products and application expertise aligned with current business strategy to address needs of researchers within protein sample prep and analysis workflow across a wide range of applications. Identify and implement new applications for existing MilliporeSigma products. Plan experiments and write protocols, report activities & results. Ensure coordination with project managers, technical leads and management through good communication. Present technical seminars at conferences, workshops and customer sites. Provide technical leadership on cross-functional teams supporting the product development process. Who You Are PhD/Masters degree in Biomedical Engineering, Biology, Biotechnology, Biochemistry, or a closely related technical field. Hands on experience across a range of life science applications – Protein preparation & analysis workflows, molecular biology, Biochemistry etc. Experience defining and balancing customer, business and operational needs, developing new products a plus. Previous experience mentoring or supervising desirable. 2+ years of experience in an academic and/or industrial lab working in protein science, biochemistry etc. Hands‑on experience across a broad range of life science applications in protein preparation and analysis. Some experience in cell biology and cell‑based assays would be an added plus. Highly organized; self-starter able to handle multiple tasks simultaneously; adapt well to change and able to prioritize multiple projects. Innovative problem solver with creative thinking skills for overcoming difficult challenges. Excellent experimental planning and data interpretation skills. Excellent communication and presentation skills. Ability to navigate ambiguity and provide clear direction in a highly dynamic and fast-paced environment, ensuring effective execution across stakeholders. Experience leading across a complex, international network of stakeholders, including Commercial, R&D, Quality, Business, Finance and Operations. #J-18808-Ljbffr
A global life sciences company is seeking a DxRM Account Manager in Carrigtwohill, Ireland. This field-based role is focused on delivering tailored solutions to customers in Industrial, Testing, Academia, and Pharma while achieving sales goals. Candidates should have a Bachelor’s degree in a scientific or technical field and at least 5 years of field sales experience. The position requires excellent communication skills, business acumen, and the ability to work autonomously while traveling to meet customers regularly. #J-18808-Ljbffr
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Role The Team Leader plays a key leadership role within the production team, balancing hands‑on involvement on the production line with guiding and supporting team members. As subject matter experts, Team Leaders ensure production activities meet safety, quality, delivery, and efficiency standards. They take the lead in troubleshooting, resolving issues, managing line schedules, and providing training on procedures. While actively contributing to the team’s daily operations, Team Leaders also hold responsibility for driving shift performance targets. Duties Accountable for overall manufacturing performance within shift on all fronts (Safety, Quality, Supply Continuity) Responsible for actively identify areas for immediate improvement and implement best practices at the team level to enhance operational efficiency and product quality. Effectively use automation tools and digital applications to streamline daily operations, providing feedback on their effectiveness and troubleshooting any issues that arise. Act as owner & collaborate with other team leads to share best practices and communicate team needs to supervisors, ensuring alignment and support across departments. Data Collection and Reporting: collect and report team performance data, using metrics to inform immediate operational decisions and drive performance improvements. Support Change Management: assist team members through changes in processes and technologies, encouraging feedback and adaptation to new methods while promoting a culture of continuous improvement. Who You Are Qualification in supervisory / management training an advantage. Diploma/Degree or equivalent with relevant experience in a GMP environment an advantage. Excellent computer skills Word, Excel, Power Point. 3 years experience within a manufacturing operation. Supervisory experience within a manufacturing operation an advantage. Knowledgeable of ISO, CE Mark and FDA standards and regulations. Knowledgeable in Lean Manufacturing, Six sigma. Green belt or blue belt an advantage. Strong leadership & people skills required. Excellent interpersonal and communication skills and ability to liaise effectively with various support groups. This role will initially be a days‑based role for training purposes but will transition to a shift‑based role. Some travel to our sister plant in the U.S. will be required. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life! #J-18808-Ljbffr
A leading life sciences company in Cork is seeking a Team Leader for their production team. This role balances hands-on involvement with guiding team members to meet safety, quality, and delivery standards. Candidates should have a diploma or degree in a relevant field, with at least 3 years of manufacturing experience, and strong leadership skills. The position will start as days and transition to shifts. The company values diversity and offers opportunities for career growth. #J-18808-Ljbffr
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Role The Supervisor will be responsible for supporting the initial Operation Readiness of the Blarney facility. In addition, the Supervisor will be accountable for the achievement of Production targets, Department metrics and key Department/Site objectives using Life Science Production System (LSPS). The Production Supervisor directs all aspects of production activity at the assigned area to ensure that the desired quantities and quality of products are manufactured on schedule in a safe manner at minimum cost. Is responsible for human resources and may be responsible for accounting and other staff functions. The Production Supervisor is initially a days based position. However, as production ramps up, the position will become a shift based position. The role may require travel to the United States for training purposes. Duties Supervision of employees, allocating work, co-ordinate training and dealing with issues as arise up to counselling stage of disciplinary process. Ensure Attendance Management policy is adhered to. Supporting the Training & Production coordinator with pre-interview, on-boarding and training activities to ensure F2.0 project and manufacturing commitments are met. Performance Management – prepare, assess and conduct all MyImpact conversations. Assist operators with developing their commitments. CORE Time & Attendance – Sign off T&A on a weekly basis in a correct and accurate manner. Responsible for on the job training and specific training as required. Responsible for assigning tasks to operator team(s) and for the material flow / work within department. Co-ordination of operator tasks to meet weekly plan. Partner with the planning department to deliver on the manufacturing plan. Accountable for physical movement and information flow of materials from order opening to order closing. Responsible for Kitting & Closing of SAP Process Orders. Responsible for adherence to Cycle Count Procedure and meeting cycle count accuracy metrics. Partner with the Quality department to ensure compliance with Quality Standards. Foster culture of right first time ensuring product quality. Ensures documentation is maintained in accordance with quality requirements & completes necessary updates as appropriate. Supporting the investigation & follow-up in relation to complaints and implements corrective & Preventative actions. Ensures Audit readiness – drives this culture and aligns this through 6S Audit approach. Supports the validation activities. Providing a safe workplace for all employees. Ensures compliance with all applicable Environmental, Health and Safety legislation & adherence to Safety procedures & requirements. Ensures that timely communication and measurement systems are in place, and active, for department metrics including, but not solely: EHS proactive reporting & appropriate, timely EHS Action close out FPQ tracking & reporting MyLearning tracking & reporting Daily OEE tracking & reporting Financial (including Absorption, Material Variance, Overtime & Disc Spend) Communicate Scorecard(s) weekly and ensure targets are met/exceeded. Foster a Culture of continuous improvement using Life Science Production System (LSPS). Using processes and daily management systems (DMS) and Leaders Standard Work. Who You Are Minimum 3 years Supervisor experience within a Manufacturing operation. Excellent computer skills (Word,Excel,Powerpoint,etc..) Excellent Operation systems knowledge (MES, SAP, LIMs, etc.) Strong knowledge of EHS, Quality, GMP standards and regulations. Strong leadership & people skills, with excellent interpersonal and communication skills and ability to liaise effectively with various support groups Strong, capable decision maker who provides clear direction to all team members including all support functions. Qualification in Supervisory / Management training desirable. Diploma/FETAC Level 7 qualification desirable. Knowledgeable in Lean Manufacturing, Six sigma (Greenbelt or Bluebelt) desired. What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring your curiosity to life! #J-18808-Ljbffr
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your role: As the EMEA Sourcing Manager (f/m) within our Global Sourcing Operations team for the Life Science division, you will lead the strategic sourcing process for key suppliers supporting our EMEA manufacturing plants. In this pivotal role, you will drive our organization's growth and innovation initiatives by collaborating closely with Category Managers to convert category strategies into actionable sourcing plans that align with our business objectives. Your responsibilities will include identifying, negotiating and managing strategic supplier relationships while ensuring that quality and performance standards are consistently met. You will oversee the development and implementation of comprehensive sourcing strategies, driving collaboration across cross-functional teams. Additionally, you will monitor supplier performance, addressing any issues promptly to maintain high standards in our sourcing lifecycle. This position offers the opportunity to influence change and improve operational efficiency, contributing significantly to our success. You will be instrumental in supporting sustainability programs and ensuring compliance with contract management processes. Your leadership will help us establish strong relationships with local and regional stakeholders. Join us in Ireland or United Kingdom for this exciting opportunity where your contributions will make a meaningful impact! Who You Are You hold a Master's degree in Business, Supply Chain Management, Life Sciences or a related field. You have a minimum of 5 years of experience in strategic sourcing or procurement within the Life Sciences, Medical Device or Pharmaceutical industries. You possess excellent negotiation and communication skills, with the ability to influence and engage stakeholders at all levels. You have a proven track record of successfully managing the end-to-end sourcing process, including supplier identification, negotiation and performance management. You demonstrate strong leadership capabilities and experience in managing cross-functional and multinational sourcing initiatives. You have advanced analytical skills and the ability to solve complex problems. You are proficient in analytical tools, including MS Office and have experience with ERP systems such as SAP or Oracle. You are a proactive team player with a focus on innovation and continuous improvement. You are fluent in English other language will be appreciated What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #J-18808-Ljbffr
A leading life sciences company seeks a Production Supervisor in Carrigtwohill, Ireland. This role involves overseeing the day-to-day production activities, ensuring targets are met, and compliance with health and safety regulations. The ideal candidate should have at least 3 years of supervisory experience in a manufacturing environment and be skilled in leadership and decision-making. The position is initially day-based but will transition to shifts as production increases, requiring potential travel for training in the U.S. #J-18808-Ljbffr
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. CSV Engineer - Blarney Reporting to the Quality Manager – Validation / Principal Validation Engineer, the Computer System Validation (CSV) Engineer is responsible for the design and execution of validation projects and strategies to support the site-based implementation of the manufacturing execution systems (MES) within the production environment. The CSV Engineer works as part of a cross-functional teams to lead and support validation activities of the MES solutions (Siemens OpCenter, AspenTech) that deliver efficient, accurate and both regulatory compliant & satisfy internal requirements qualifications. Duties & Responsibilities Authoring, reviewing and executing Computer System Validation (CSV) plans, protocols and reports in alignment with GAMP 5 and applicable regulations. Ensure site consistently interpret and implements corporate policy across all Computer Systems areas. Execute and complete validation activities from software install to business release for site systems including MES solutions (Siemens OpCenter, AspenTech) in accordance with Validation Master Plans, company policies and project schedules. Participate in cross-functional teams to establish validation strategies and objectives to support new systems and system upgrades. Maintain ongoing understanding and knowledge of requirements for validation in compliance with applicable regulations and guidance documents, provide updates to department management and cross-functional teams. Participate in the review of validation practices and trends, identify opportunities for continuous improvement and complete improvement projects. Ensuring change control processes are appropriately followed for validated systems. Lead and co-ordinate Risk Mitigation initiatives such as FMEA and Risk Assessments for new systems and upgrades. Completes associated new systems and system upgrades Change Control activities in accordance with Quality Standards and Practices. Providing support for CSV activities during internal audits, customer audits and regulatory inspections. Maintaining and updating validation documentation to ensure audit readiness. Monitor the progress of validation projects to ensure adherence to schedule and provide regular stakeholder updates. Ensure thorough investigation of Quality and Validation issues using Root Cause Analysis methodology and implementation of robust corrective and preventative actions to prevent re-occurrence. Reports and escalates critical quality issues to the appropriate level of quality management for approval of final resolution. Adhere to all company EHS guidelines and Quality procedures. Candidate Requirements B.Sc. in an appropriate Computer Science/Engineering or related discipline Minimum 5-8 years’ experience implementing IT solutions, systems integration, support & validating IT applications and interfaces within the pharma/medical device or similar industry Proven experience supporting validation of systems such as MES solutions (Siemens OpCenter, AspenTech) Working knowledge of 21 CFR Part 11, Annex 11, GAMP 5 and Data Integrity principles Proficiency in programming languages and MES platforms (e.g., AspenTech, Siemens, Rockwell) Proven technical experience of writing validation plans, requirements gathering, design documentation, system configuration, system testing and troubleshooting Strong oral, presentation and written communication skills are required, with proven ability to communicate and build relationships cross-functionally Demonstrated success working in a team environment Effective time-management skills to meet project schedules Self-motivated, detail-oriented and excellent organizational and time management skills What we offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! #J-18808-Ljbffr
