A biotechnology company in Cork, Ireland is seeking a professional for laboratory maintenance and quality control. Responsibilities include coordinating equipment maintenance, ensuring compliance with GMP standards, and managing documentation. Ideal candidates have 2-4 years of GMP experience, a degree in Life Sciences, and strong skills in record keeping and communication. This position offers the opportunity to contribute to innovative drug discovery in a supportive environment. #J-18808-Ljbffr
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. About Commercial Our Commercial organization leads our global sales and marketing strategies around the world. Our integrated team continues to solidify BioMarin’s commercial presence in the United States and Europe and is rapidly growing in other regions, such as Latin America, the Middle East and Asia-Pacific. Senior Manager –Technical Accounting, Risk and Compliance Temporary Contract - Dublin BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life‑threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind. By providing a foundation for all operations company wide, BioMarin’s General and Administrative teams support our mission of providing first and best in class therapeutics to patients who live with rare diseases. Our teams include groups such as finance, legal, human resources, corporate compliance and ethics, and information technology. Come join our team and make a meaningful impact on patients’ lives. SUMMARY DESCRIPTION BioMarin is seeking a highly motivated Senior Manager with solid experience in applying accepted accounting principles managing across multiple countries in the EMEA region. The Senior Manager will be able to work across teams to establish appropriate accounting control procedures and monitor compliance with accounting standards. This position will be a key member of a cross‑functional, multi‑national, finance team supporting General Ledger accounting, Corporate Accounting and Tax. Motivated self‑starter who is detailed, results and process oriented with a focus on effective and efficient improvements Organized individual with the ability to manage multiple priorities while maintaining high performance standards Superior problem solving and analytical skills and ability to work in a highly visible, deadline‑oriented position and environment Strong communication and people skills, comfortable working with a cross functional and collaborative team and effectively able to deal with all levels of personnel RESPONSIBILITIES Technical Accounting Drafting and distributing technical accounting memos for complex transactions and Control deviations Identifying and documenting differences in GAAP reporting (especially between US GAAP and IFRS) Devising step plans for corporate transactions, such as dividends, intercompany loans, etc. Liaising with auditors on technical accounting queries SOX Audit coordination Supporting the planning of the group SOX audit from a regional perspective Managing and monitoring risk control matrices Regional SOX Coordinator on the Global team Financial Statements Ensuring timelines for statutory audits and financial statements are maintained by internal and external stakeholders Liaising with cross functional teams to ensure deliverables are met Reviewing financial statements for accuracy and completeness Managing and driving accountability through the performance dashboard Review of outsourcing and audit contracts Leading planning activities with EMEA auditors and advisors Risk register Scheduling and managing the monthly risk register meetings Driving engagement through the meeting Management of the risk register dashboard Budgets Managing the budgets for audits and outsource providers Reviewing reconciliations of monthly accruals to budget Process improvement Make meaningful contributions to introducing efficiencies in the statutory reporting process Document and map out processes for statutory reporting General Contribute to team effort and assist co‑workers as needed Work closely with Finance colleagues both locally and globally, adhering to global deadlines Assist with ad‑hoc financial analysis, queries and EMEA Finance activities as required EDUCATION University degree in Business, Finance or Accounting Qualified Accountant EXPERIENCE Minimum 8‑10 years relevant experience in similar role is essential Knowledge of both US GAAP and IFRS is advantageous Familiarity with Sarbanes Oxley and internal controls SAP experience is desirable Strong interpersonal, analytical thinking and organisational skills Proficiency in PC skills (particularly Word, Excel, and Teams) Ability to work independently and within a team Ability to work under pressure and to handle several projects at once Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #J-18808-Ljbffr
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well‑understood biology and provide an opportunity to be first‑to‑market or offer a substantial benefit over existing therapeutic options. About Commercial Our Commercial organization leads our global sales and marketing strategies around the world. Our integrated team continues to solidify BioMarin’s commercial presence in the United States and Europe and is rapidly growing in other regions, such as Latin America, the Middle East and Asia‑Pacific. Global OTC Operations Team is part of our Global Finance Organization, with team members in Dublin and California. The team has responsibility and audit & SOX compliance accountability for all activities related to Accounts Receivable, Billing, Credit and Collections Management, and also provides oversight to the transactional execution of OTC business processes and facilitates OTC Governance Forums across all levels of the organisation. The OTC Operations Team also focuses on driving continuous process analysis and improvement to deliver efficiencies and scale in support of ongoing business growth. Job Title Account Receivable Analyst (Intercompany) Location Dublin, Ireland Summary Based in Ireland, this role reports to the Associate Director – Order to Cash Finance Operations and supports our Global OTC Operations. Key Responsibilities Intercompany: Completing cash application for all intercompany payments ensuring these are completed in a timely manner and to period close deadlines. Regular review of Intercompany ledger to identify issues and next steps. Investigating and resolving queries in an efficient and timely manner. Period Close & AR Reporting Activities: Assist with timely Month End AR Ledger Close / Month End Close. Perform Weekly/Monthly Reconciliations. Support the year‑end financial statement audit process and the SOX audit process. Continuous Improvement Activities: Identify opportunities for continuous process improvements and innovative solutions so the team can operate in an efficient manner. Proactively identify, rectify and follow‑up on errors and causes of errors while managing the quality and development of financial accounts, systems, and processes. Support project and continuous improvement tasks as required. General: Assist with ad‑hoc OTC Global Operations activities. Ability to communicate in a clear and concise manner. Contribute to team effort and assist co‑workers as needed. Education University degree in Business, Finance or Accounting, or equivalent experience. Experience Strong interpersonal skills with the ability to work independently and within a team. Proficiency in PC skills (particularly Word and Excel). Attention to details is key. Strong problem analysis and problem‑solving skills. Ability to use own initiative to make decisions based on own research. Knowledge of SAP and cash application a plus. Note This description is not intended to be all‑inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer / Veterans / Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #J-18808-Ljbffr
A biotechnology company in Dublin is seeking an Account Receivable Analyst to support financial operations. The role involves completing intercompany payments and assisting with month-end close processes. The ideal candidate will have a degree in Business, Finance, or Accounting, with strong interpersonal and problem-solving skills. Attention to detail and proficiency in Word and Excel are essential. This position offers opportunities for process improvement and innovative solutions within a dynamic team environment. #J-18808-Ljbffr
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. About Technical Operations BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting‑edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Responsibilities Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the BioMarin’s Enterprise Computerized Maintenance Management System (CMMS). Responsible for the completion of QC equipment related documentations. Perform change request using the BioMarin’s Enterprise Quality Management System (Trackwise). Maintain vendor service contracts using BioMarin’s SpringCM system. Maintain good working relationships with vendors to ensure vendor meets BioMarin’s current and future needs. Work with vendors to troubleshoot equipment. Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts. Maintain the electronic and paper inventory for equipment qualification packages. Perform equipment inventory reconciliation with physical assets in each laboratory; assessing the current and future suitability. Requirements 2-4 years of experience working in a GMP environment. BS/BA in Life Sciences or equivalent experience. Some experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices. Understanding of GxP guidelines. Must have excellent record keeping, written and verbal skills. Ability to perform most tasks with minimal supervision. Computer literacy is required. Experience with Microsoft Excel and Word is required. Note Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #J-18808-Ljbffr
A leading biotechnology company in Dublin seeks a Senior Manager for Technical Accounting, Risk, and Compliance. This role involves establishing accounting controls, managing SOX audits, and collaborating with cross-functional teams to ensure compliance. Candidates should have a degree in Business or Accounting and 8-10 years of relevant experience. The position requires strong analytical and organizational skills, along with proficiency in tools like SAP and Excel. The company fosters innovation in developing therapies for patients with rare genetic diseases. #J-18808-Ljbffr
A global biotechnology company in Ireland is seeking a Senior Engineer for Drug Product to support drug product filling operations and lead technical initiatives across a matrix team. The ideal candidate will have a solid background in MSAT or process development and experience with biologic drug products. This role requires excellent organizational and communication skills to ensure compliance with regulatory standards while facilitating investigations and process improvements. #J-18808-Ljbffr
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well‐understood biology and provide an opportunity to be first‑to‑market or offer a substantial benefit over existing therapeutic options. About Technical Operations BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting‑edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinate the worldwide movement of our drugs to patients. Position Overview Senior Engineer, Drug Product – Cork/Dublin Technical Development are hiring a Sr Engineer with the following duties: Duties Technical SME for drug product (DP) supporting filling operations, working in a matrix team environment with process development, QA, QC, analytical sciences, packaging, supply chain, and regulatory teams to achieve project objectives. Supporting both Global External Operations (GEO) and Shanbally teams. Develop process comparisons, risk assessments, manage DP technical and manufacturing risks and identify appropriate mitigations. Author technical reports to support DP process and product characterisation. Manage change control, deviations, and CAPAs through the quality management system until closure. Facilitate investigations, root cause analysis for deviation resolution, data gathering/analysis, and provide technical assessments for deviations. Initiate and lead process improvement projects, involving cross‑functional teams. Support the technical delivery of new product introductions and tech transfer projects by closely collaborating with cross‑functional project teams, ensuring compliance with specifications, regulatory guidelines, and right‑first‑time delivery. Assist with PPQ campaign readiness and provide in‑person, on‑the‑floor execution support for technical runs and PPQ campaigns as required. Support on‑site implementation of changes and DP launch activities. Support aseptic filling operations (vials and pre‑filled syringes) for technology transfers and life‑cycle management, overseeing new product introductions from development batches to approval and commercialization. Assist with regulatory inspections and present technical topics related to process aspects of assigned products when necessary. Ensure a thorough understanding of all quality policies and BioMarin system items as outlined in the training curriculum. Other duties as assigned. Skills Strong understanding and hands‑on experience in MSAT or process development or technology transfer, background in large‑scale processing of biologic drug products. Possess a strong understanding and hands‑on experience in MSAT, process development, or technology transfer, with a background in large‑scale processing of biologic drug products. Have a solid understanding of regulatory requirements and guidelines. Proficient in technical writing. Demonstrated ability to build strong partnerships and work effectively with diverse team members in a dynamic environment. Excellent organizational, interpersonal communication, and problem‑solving skills. Capable of identifying, communicating, and implementing continuous process improvements. Ability to multi‑task and manage tight timelines in a fast‑paced environment. Able to work on the manufacturing floor for extended periods during the execution of technical protocols. Excellent written, verbal, and presentation communication skills. Strong analytical skills and sound judgment. Effective decision‑making skills, with the ability to negotiate and balance decisions and priorities across multiple stakeholders’ needs. Proficient in MS Office: Word, Excel, Outlook, PowerPoint, MS Project, etc. Education and Experience A degree in engineering or science with relevant experience in the biotech/pharmaceutical field. Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer / Veterans / Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #J-18808-Ljbffr
A leading biotechnology company in Ireland seeks a QA Site Inspection Manager to ensure ongoing compliance with GMP regulations. This hybrid position requires 10–15 years in GMP-regulated environments, a bachelor's in relevant fields, and leadership experience. The role includes developing inspection readiness strategies, guiding stakeholders on regulatory trends, and maintaining site licenses. This position offers an opportunity to impact patient lives through quality assurance in therapeutics. #J-18808-Ljbffr
A global biotechnology company is seeking an Engineering Validation Associate in Cork, Ireland. The role involves planning and implementing validation activities in a GxP regulated environment, developing validation plans, and ensuring compliance with industry standards. Ideal candidates will have 8-10 years of industry experience and a background in validation processes. This position contributes to the development and quality of transformative medicines, maintaining high safety and regulatory standards. #J-18808-Ljbffr
