A leading biopharmaceutical company in Ireland is seeking a Manager for External Manufacturing Finance. This role involves managing finance functions related to external manufacturing and collaborating with cross-functional teams across the US and Europe. The ideal candidate will have a strong accounting background with at least 3 years of experience in financial analysis, excellent Excel skills, and the ability to build relationships with stakeholders. Benefits include a competitive salary, bonuses, and access to company health insurance and gym facilities. #J-18808-Ljbffr
The Role Manager External Manufacturing Finance, based in Ireland, reporting directly to the Associate Director for External Manufacturing. The role involves interaction with cross‑functional colleagues in the US and Europe and offers flexibility to work remotely up to 50% of the time. Responsibilities Key colleague in the External manufacturing finance team responsible for Subcontracting/PPV/Freight Month end reporting and commentary, variance and trend analysis Preparation and timely submission of ExM Budget and Projections Prepare product costing across a significant number of materials Serve as Virtual Plant Team finance representative to ensure strong business partnering Preparation of tolling reconciliations in compliance with corporate policies and procedures Identify financial risk and quantify operational risk Ensure SOX control compliance where applicable Facilitate and support internal and external audits as required Competencies & Requirements Qualified accountant with strong knowledge of costing and financial analysis, accounting principles, and internal controls, with at least 3 years post‑qualification experience Strong Excel skills essential; knowledge of SAP ERP desirable Proven track record of delivering high‑quality results Ability to develop and maintain strong relationships with internal and external stakeholders Excellent organisational skills and effective communication of ideas Network building skill to obtain and disseminate critical information to the External Manufacturing Business Unit Demonstrated ability to work in cross‑functional teams in a complex, changing environment and deliver value‑added results Strong analytical and problem‑solving skills in execution of job responsibilities Benefits Competitive salary and annual bonus Pension contribution Family health insurance 27 days of annual leave Access to on‑site gym and life assurance R1601484 Manager External Manufacturing Finance We are an equal‑opportunity employer. #J-18808-Ljbffr
A leading biopharmaceutical company in Dublin is seeking an experienced professional to provide strategic leadership in clinical supply. The role requires 15+ years in related fields and a bachelor's degree. Key responsibilities include overseeing workload, facilitating discussions, and acting as the primary coordination point for studies. The company offers a comprehensive benefits package, including health coverage and flexible time off. #J-18808-Ljbffr
Key Responsibilities Provide TA-level strategic direction and operational leadership across the portfolio, ensuring alignment with clinical development priorities. Facilitate regular strategic discussions with TA Leads and stakeholders to ensure alignment, rapidly resolve issues, anticipate resource swings, and share forward‑looking insights. Serve as the TA's primary point of coordination for new assets, new studies, and incoming work, ensuring rapid assessment, appropriate coordination, and structured assignment paths. Own and oversee TA‑level capacity planning and workload balancing, including intra‑ and inter‑TA resource alignment across CSLs, TSMs, and supporting roles. Own and leverage Control Tower / CSSSA and TA‑level performance data to monitor KPIs, anticipate demand, and drive performance improvement. Lead the intake process for all new requests (CMC, GDO, IRT, etc.), including chairing intake meetings and making CSL/TSM assignment decisions based on expertise, capacity, study prioritization, and other relevant managerial/operational factors. Act as first‑line decision‑maker for cross‑study or cross‑asset conflicts, study prioritization, escalation/acceleration handling, and trade‑off alignment across the TA and between TAs, as needed. Anticipate risks and proactively intervene or escalate to avoid near misses, delays, or supply disruptions across the TA. Lead root cause analyses when misses, delays, or supply disruptions occur. Serve as the TA's senior representative during portfolio reviews, scenario planning, pipeline acceleration discussions, and integration activities (e.g., due diligence, new modalities). Contribute to improving CD&OP maturity by reinforcing consistent inputs, process discipline, and cross‑functional engagement. Tactically ensure the appropriate projects are being escalated up the CD&OP process to achieve rapid resolution. Own TA‑level KPI frameworks, dashboards, and performance metrics to monitor execution, identify risks, and drive continuous improvement. Drive data‑enabled decision‑making, leveraging AI‑enabled insights and validated data sets to guide operational improvements, assess resource allocations and inform timely, actionable future planning. Partner with other Clinical Supply Team Leads to ensure intra‑ and inter‑TA harmonization, alignment, coordination, and continuous improvement. Oversee TA‑level compliance with GxP, Quality, and regulatory inspection expectations ensuring CSLs, TSMs, and other staff maintain timely and accurate data, forecasts, systems, and documentation. Provide direct line management, coaching, and development for assigned staff, and drive engagement and performance across TA teams. Qualifications & Experience Bachelor's degree in Pharmacy, Engineering, Supply Chain, Life Sciences, or related field. 15+ years of clinical supply chain, clinical operations, technical operations, or related biopharmaceutical leadership experience. Demonstrated expertise in end‑to‑end clinical supply planning, investigational product management, and global study execution. Demonstrated strategic planning and leadership skills. Knowledge of effective executive communications, stakeholder management, and partner/customer engagement. Strong understanding of drug development, clinical operations, CMC, regulatory expectations, and GxP quality systems. Proven ability to lead matrixed teams, manage senior stakeholders, and influence without authority across global and cross‑functional environments. Advanced analytical skills with experience using digital tools, dashboards, AI‑enabled insights, or supply chain performance data. Demonstrated success providing change leadership within dynamic, complex, fast‑paced environments. Ability to recruit, select, coach, engage, and develop team members. Preferred Qualifications Master's degree (MBA, MS, PharmD, or related discipline). Experience leading or implementing large‑scale process, digital, or organizational transformations. Prior leadership of global clinical supply teams. Experience in portfolio‑level planning, scenario modeling, or pipeline acceleration initiatives. Familiarity with enterprise digital platforms (IBP, Control Tower, Lighthouse, etc.). Excellent cross‑functional negotiating and influencing skills. Compensation Overview Madison – Giralda – NJ – US $221,970 – $268,974 Princeton – NJ – US $221,970 – $268,974 Starting compensation range for this full‑time role is listed above. Additional incentive cash and stock opportunities, based on eligibility, may be available. Final, individual compensation will be determined by demonstrated experience. Benefits Health coverage: medical, pharmacy, dental, and vision care. Well‑being support programs such as the BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs. Financial well‑being and protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Paid Time Off and Work‑Life Benefits US Exempt Employees enjoy flexible time off (unlimited, with manager approval), 11 paid national holidays (excluding Phoenix, AZ, Puerto Rico or Rayzebio employees), and additional optional holidays as specified. Extra time off options include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs. Global employees eligible for a yearly global shutdown between Christmas and New Year's Day. Equal Employment Opportunity Statement BMS considers qualified applicants with arrest and conviction records, pursuant to applicable laws in the applicant's area. For additional information regarding EEO and disability accommodations, see BMS EEO statement and accessibility page. Data Protection Statement BMS will never request payments, financial information, or social security numbers during the application or recruitment process. For information on protecting yourself from fraud, see the BMS fraud‑protection page. All data processed in connection with this role will be treated in accordance with applicable data privacy policies and regulations. #J-18808-Ljbffr
A leading pharmaceutical company based in Dublin is seeking a Manager for External Manufacturing Finance. The role includes handling subcontracting finance, month-end reporting, and preparing budgets. Candidates must be qualified accountants with strong finance analysis skills and at least 3 years of post-qualification experience. This position offers remote work up to 50% of the time and includes competitive salary benefits, health insurance, and generous leave allowances. #J-18808-Ljbffr
Working with Us Challenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb Ireland Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. Ireland is home to External Manufacturing’s global headquarters, the business unit responsible for the management of manufacturing contract operations (CMO’s) and ensuring reliable supply of product to patients across the Bristol Myers Squibb global network. This includes management of, and working in conjunction with, third‑party contract manufacturers and internal manufacturing sites. In Ireland, External Manufacturing has two sites; Global Headquarters based in Dublin 15 and a distribution centre in Shannon, Co Clare. The Role BMS External Manufacturing is looking to recruit a Specialist, Supply Chain Operations for a fixed term contract of twelve months reporting to the customer service team lead. Main responsibility is to provide a key link in Supply Chain between customers and inter‑company and third‑party supply sites and markets. Order processing and invoicing. Key Duties And Responsibilities Manage Operations: Liaise with principals’ purchasing, finance departments and fiscal reps to perform Supply Chain Operations activities on their behalf. Provide a key link in Supply Chain between inter‑company and third‑party supply sites and markets. Ensure that customer and supply sites comply with business and tolling rules. Resolve discrepancies in quantity and timing of market orders. Receipt and entry of market orders as per business rules. Receipt and process supplier invoices and follow up on price discrepancies, and payment queries. Accurate receipt and process tolling fee invoices. Perform all activities in accordance with Good Distribution Procedure. Issue invoices to markets. Issue required shipping documents, certify with local Chamber of Commerce and legalise with relevant embassies as required. Liaise with freight forwarder/logistics for outbound shipments and update freight tracker/register if applicable. Approval or sign‑off of redeployment/rework on behalf of principal. Co‑ordinate redeployments/reworks and ensure that the costs are back‑charged to the appropriate party. Liaise with QC for testing, release and generation of CoAs for API if applicable. Liaise with QC for QP inspection and release of drug products. Manage Information: Assist and support master data related to customers, contracts and BOMs. Use reports to monitor and ensure data integrity if applicable. Receive and forward customer complaints as per established procedures. Follow up and expedite for prompt resolution. Manage Financial Activities / Compile Financial Reports: Perform all SAP transactions in a compliant manner. Meet finance deadline for month‑end and year‑end sales reporting. Provide supporting documentation for financial audits as requested. Team work: Work with External Manufacturing organisation to support implementation of new supply models. Qualifications, Knowledge and Skills Required Experience working in a multinational company; preferably in an export department. Three years’ experience in a multinational supply chain environment, warehouse transactional or any other related experience. Supply chain or business qualification – diploma standard. Deliver results on time in a pressurised environment. Must be flexible and be able to deal with changing priorities. Demonstrate efficiency in supply chain administration, accuracy and timeliness of order processing. Set demanding goals for themselves while maintaining accuracy and a high level of productivity. Follow through commitments to customers without detriment to the team or company. Exhibit strong interpersonal and communication skills when dealing with colleagues and external customers. Ability to prioritise, organise and manage multiple tasks to tight deadlines. Exhibit a strong ability to use computer systems efficiently, workable knowledge of ERP system, ideally SAP. Create and maintain strong working relationships within the BMS organisation and externally with trade customers and suppliers. Understand BMS supply chain, products and markets. Adapt quickly to the demands of the job and show the ability to learn quickly. Adhere to all regulatory, finance, EHS and security compliance procedure. Knowledge of supply chain operations standards. Knowledge of order processing and invoicing activities. Why you should apply You will help patients in their fight against serious diseases. You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days of annual leave, access to BMS Cruiserath on‑site gym and life assurance. On‑site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site‑essential, site‑by‑design, field‑based and remote‑by‑design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role. Site‑essential roles require 100% of shifts onsite at your assigned facility. Site‑by‑design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive company culture. For field‑based and remote‑by‑design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People With Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Important Additional Information If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https://careers.bms.com/california-residents/ . Contact R1601407 Supply Chain Operations Associate #J-18808-Ljbffr
The Role Manager External Manufacturing Finance, based in Ireland, reporting directly to the Associate Director for External Manufacturing. The role involves interaction with cross‑functional colleagues in the US and Europe and offers flexibility to work remotely up to 50% of the time. Responsibilities Key colleague in the External manufacturing finance team responsible for Subcontracting/PPV/Freight Month end reporting and commentary, variance and trend analysis Preparation and timely submission of ExM Budget and Projections Prepare product costing across a significant number of materials Serve as Virtual Plant Team finance representative to ensure strong business partnering Preparation of tolling reconciliations in compliance with corporate policies and procedures Identify financial risk and quantify operational risk Ensure SOX control compliance where applicable Facilitate and support internal and external audits as required Competencies & Requirements Qualified accountant with strong knowledge of costing and financial analysis, accounting principles, and internal controls, with at least 3 years post‑qualification experience Strong Excel skills essential; knowledge of SAP ERP desirable Proven track record of delivering high‑quality results Ability to develop and maintain strong relationships with internal and external stakeholders Excellent organisational skills and effective communication of ideas Network building skill to obtain and disseminate critical information to the External Manufacturing Business Unit Demonstrated ability to work in cross‑functional teams in a complex, changing environment and deliver value‑added results Strong analytical and problem‑solving skills in execution of job responsibilities Benefits Competitive salary and annual bonus Pension contribution Family health insurance 27 days of annual leave Access to on‑site gym and life assurance R1601484 Manager External Manufacturing Finance We are an equal‑opportunity employer. #J-18808-Ljbffr
A multinational biopharmaceutical company in Dublin is seeking a Specialist in Supply Chain Operations for a fixed-term contract. The successful candidate will serve as a vital link between customers and supply sites, handling order processing and invoicing. Required are three years of experience in a supply chain setting and a relevant diploma. The role emphasizes effective communication, flexibility, and proficiency in SAP. A competitive salary and benefits package are provided, including health insurance, annual leave, and a bonus. #J-18808-Ljbffr
A leading biopharmaceutical company in Ireland is seeking an experienced Maintenance Engineer to enhance safety and reliability within their Drug Product maintenance team. This role involves supporting equipment installation and ensuring compliance with regulatory standards throughout operations. Candidates should possess a Level 8 Engineering qualification and at least 3 years of relevant experience. The job emphasizes problem-solving and teamwork, aiming for continuous improvement in maintenance processes. #J-18808-Ljbffr
Overview Position: Vice President, GBU Quality Challenging. Meaningful. Life-changing. Bristol Myers Squibb offers a work environment where unique, impactful work happens daily across departments. This role focuses on shaping the Quality strategy for the Global Business Unit (GBU) Manufacturing Quality Network, ensuring cGMP compliance and the safety, efficacy, and quality of bio and pharma products. You will lead quality operations across manufacturing, laboratory operations, and product release/certification, interfacing with internal and external manufacturing. The role requires collaboration with Global Manufacturing and Supply Chain functions and is part of the Global Quality Leadership Team (GQLT) and the GBU Leadership Team. You will manage a team of managers, including Site Quality Heads of internal sites and other Quality Leaders supporting compliance and network projects. The position supports overall GBU Network Strategy and operational performance and strives to build an excellent infrastructure (people, processes, systems) to handle moderate to high complexity quality and compliance responsibilities to ensure product quality and supply continuity. Key Responsibilities Supports the development, direction, and execution of the quality strategy for the GBU (Biologics & Pharma) manufacturing organization. Provides leadership for a multi-functional group of quality professionals aligned with company culture and regulatory trends to achieve a uniform quality strategy, and enables quality activities for compliance and network projects. Ensures a robust and effective quality management system is implemented according to global standards to achieve the GBU Manufacturing quality objectives. Advances the suitability and effectiveness of the quality management system and GMP compliance through participation in required quality management reviews. Deploys Quality Risk Management techniques for quality oversight and problem resolution in partnership with Manufacturing/Supply Management and Quality. Manages/supports resolution of quality and technical problems within the GBU, including internal and external manufacturing, aligned with global standards. Supports audits and Health Authority inspections for GBU sites, including HA responses and CAPAs; ensures critical issues are escalated and resolved within defined timelines. Ensures quality governance through KPI reviews, metrics, process indicators, and quality system signals; initiates and follows up on corrective actions. Oversees GMP follow-up actions for audit/inspection observations as per the Quality Management System. Provides quality oversight and adequate resourcing for complex projects (transfers, launches, due diligence) to ensure QMS compliance and issue escalation/resolution. Provides SME input to BMS policies, directives, and SOPs related to quality compliance when required. Leads communication and develops strategies with stakeholders from Manufacturing, SB&E, Supply Chain, Regulatory, Project Management, and Operations. Builds organizational capability, recruits and develops global talent, and fosters a high-performance culture within the GBU Quality organization. Coaches and mentors direct reports to build a highly capable team capable of meeting business needs. Supports deployment of operational excellence strategies within Quality GBU Manufacturing. Prepares and manages the Quality GBU organizational budget. Champions the development and implementation of innovative and digital solutions across the GBU Quality team and organization. Qualifications & Experience B.S. degree in relevant Science or Engineering. Advanced degree preferred (MBA, MS or PhD). 20+ years of experience managing quality and compliance organizations. Proficiency in quality compliance processes and regulations (e.g., cGMP/GDP for External Manufacturing QA). Thorough understanding of policy/regulatory requirements and their relation to product quality investigations. Technical expertise in pharmaceutical/biological manufacturing, analyses, microbiology, statistics, and quality control/QA processes. Excellent communication and interpersonal skills to interface with internal and external stakeholders at all levels. Proven track record delivering results, proactive in compliance remediation activities related to regulatory actions. Strategic thinker with strong business acumen and ability to see end-to-end enterprise impact. Strong influencing/negotiation skills in a matrix environment. Ability to interact with senior leaders and act on behalf of GQ (Internal Sites) in a matrix environment. Judgment to make sound decisions from analyzed information; ability to build relationships and lead large/complex programs across diverse teams. High attention to detail, adaptable to changing environments and priorities; strong planning and organization skills. Enterprise-focused with a bias for bold decisions that improve organization-wide performance; external market awareness to inform strategy. Innovative leadership and talent development mindset; authentic leadership qualities; capable of developing talent for long and short-term needs. Compensation & Benefits Compensation: $333,760 - $404,440 (base). Starting compensation depends on skills, location, and experience. Eligible for additional incentive cash and stock opportunities where applicable. Benefits: Benefits vary by location and eligibility. For details, visit careers.bms.com/life-at-bms. Work-Life and Other Information On-site/Work Model: Site-essential, site-by-design with hybrid options where applicable; travel may be required for field-based work. Uniquely Interesting Work and Life-changing Careers aligned with Transforming patients' lives through science. Equal Employment Opportunity (EEO) and data protection statements are available on the careers site. Legal and Accessibility Supporting People With Disabilities: BMS provides reasonable accommodations in recruitment and employment; inquiries to adastaffingsupport@bms.com. See the EEO/accessibility page for more details. Candidate Rights: BMS considers qualified applicants with arrest and conviction records as required by law. Data Protection: We will never request payments or sensitive information during the application process. Visit careers.bms.com/fraud-protection for more information. All data processed in relation to role applications will follow applicable data privacy policies. Note If you believe information is missing or incorrect on this posting, contact TAEnablement@bms.com with the Job Title and Requisition number for review. Status inquiries should be directed to Chat with Ripley. #J-18808-Ljbffr
