A leading pharmaceutical company in Dublin is seeking a Manager of Fixed Assets to oversee global fixed asset processes and lead a dedicated team. This role involves ensuring compliance with US GAAP, improving processes, and mentoring staff. Ideal candidates will have a Bachelor's degree in Finance or Accounting and at least 8 years of management experience. This is a hybrid position with on-site work required for at least 3 days each week. #J-18808-Ljbffr
Manager, Fixed Assets Join to apply for the Manager, Fixed Assets role at West Pharmaceutical Services. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War II. Through our work to deliver thousands of life‑saving and life‑enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. How will yours help write our future? Job Summary Manager, Fixed Assets is a global position which will play a pivotal role in West’s capital expenditure process, being accountable for the performance and output of the global team while also providing technical guidance to staff and key stakeholders around the globe. Reporting to, and working closely with, the Director, Accounting, in this role you will be responsible for leading and managing the Global Fixed Asset Team under GFS with team members located both at the GFS Ireland site and also around our global regional locations (Europe & Americas). Responsibilities Responsible for the end to end Global Fixed Asset process Operating as a Subject Matter Expert for the global Fixed Asset Team by leading and overseeing activities performed and delivered at a consistently high level. Lead the global Fixed Asset team through period‑end closings within company deadlines while remaining compliant to West, SOX, GAAP policies and regulations Collaborating with a broad range of stakeholders including local market FP&A, Operations, Engineering, Maintenance, Senior management, and internal/external auditors. Actively oversee the review and management of the AUC/CIP balances to ensure accurate and SOX compliant reporting and accounting. Work closely with finance transformation team and IT team to bring efficiencies in the fixed asset processes. Ensuring the month‑end account reconciliation process is completed in a timely and accurate fashion with adequate supporting documentation. Initiate and drive global process improvements to standardize & harmonize processes and achieve superior levels of efficiency realizing reduced cost benefits to West. Lead in the delivery of internal and external reporting of Fixed Asset balances Represent the GFS organization on various projects and systems initiatives liaising closely with the Consolidations team, Technical Accounting and Group reporting to ensure overall consistency of process. Supporting the migration of the fixed asset activities into GFS from other business units / locations Knowledgeable in lease accounting as per US GAAP Statutory reporting oversight for all asset related balances on the global balance sheet Other duties as assigned Additional Responsibilities People Manage a team and is responsible for coaching and mentoring Focus on talent development, building a strong team Develop a customer‑centric culture in your team with highly collaborative relationships with the relevant stakeholders Ensure that company financial records are maintained in compliance with company policies and US GAAP and SEC reporting requirements Accountable for ensuring that company policies and procedures (internal controls) are implemented to provide reasonable assurance that the company assets are protected Support the Sarbanes Oxley activities relative to internal controls documentation and testing and segregation of duties Liaise with internal and external auditors Technology and Service Report agreed key performance indicators Support in preparing reports in PowerBI Education Bachelor's degree in Finance or Accounting or equivalent experience Work Experience Minimum 8 years of experience required Prior SAP implementation experience preferred Preferred Knowledge, Skills and Abilities Public Accounting background Previous Shared Service Centre with multinational publicly quoted company experience Working knowledge of US GAAP Proficient in SAP or similar ERP Proficient in MS Office applications Experience of BI tools an advantage Demonstrated ability to form, lead and develop high‑performing teams Excellent communication and leadership skills i.e. ability to communicate and work effectively with a wide range of region, division and corporate functions Able to manage multiple priorities effectively, while managing ambiguity and adapting to changing business needs and priorities Project management, meeting facilitation, written/oral communication and presentation skills Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description Able to comply with the company’s safety policy at all times Able to comply with the company’s quality policy at all times License and Certifications Qualified accountant i.e. ACA, ACCA, CIMA or CPA Additional Requirements Must work constructively in an environment that may be stressful due to competing resources while at all times maintaining company confidentiality. Must be able to work scheduled work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Travel Requirements 10%: Up to 26 business days per year Physical Requirements Sedentary‑Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. What We Offer This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post‑offer background screening and/or drug screening. #J-18808-Ljbffr
Select how often (in days) to receive an alert: Requisition ID: 71493 Date: Sep 18, 2025 Location: Dublin, Northern district, IE Department: Quality Overview This is a hybrid position (3 days per week) working in our office at Dublin, Ireland. Candidates applying must be residing within a 50-mile commutable distance to the job location. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary In this role you will be responsible for performing Supplier Quality activities associated with external suppliers. This role performs activities to ensure West supplier’s maintain compliance with West’s procedures and policies. You will interface with R&D, Sourcing, Design Quality, Regulatory and Operations Quality to drive improved supplier quality performance. Essential Duties and Responsibilities Establish and successfully execute supplier management plans which will align to overall business objectives Maintain a strong collaborative partnership with external suppliers and cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs Additional Responsibilities Monitor supplier performance including incoming failures, manufacturing yields and field failures to drive Supplier Corrective Action Reports (SCARs) Execute Supplier Corrective Action Requests (SCAR) with suppliers, ensuring effective and timely closure Work with suppliers, R&D, and Sourcing on continuous improvement of supplier performance including supplier change request Evaluate potential new or future suppliers and support supplier selection process with the cross-functional team Participate in cross-functional teams of design engineering and quality engineering to work with suppliers during product development and ensures agreement for manufacturable, cost-effective designs Approves components for use in products by driving Product Approval activities with the suppliers Supports Supplier evaluation, audit management and related records Supports the evaluation and development of Quality Agreements and purchasing specifications with suppliers Support the development of an Incoming Inspection strategy on purchased products Education Bachelor's Degree In Engineering or Science required Master's Degree In Engineering or Science preferred Work Experience Bachelor’s degree in engineering or related science Minimum 5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry Experience working with suppliers and supplier engagement activities Preferred Knowledge, Skills and Abilities Knowledge of sterilization process is preferred Knowledge of cGMP, cGDP, relevant ISO standards, medical device requirements and other international regulations Familiarity with MasterControl, SAP and working knowledge of statistical data analysis Fluent in English Thorough understanding of validation activities and risk management principles and techniques Strong problem-solving and critical thinking skills Negotiation skills and collaborating with suppliers Ability to work under high volume production and fast changing environment Willingness to work in a cross-functional team with different time zones Able to comply with the company’s safety policy at all times. #LI-AP1 #LI-HYBRID Travel Requirements 20%: Up to 52 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening. #J-18808-Ljbffr
Select how often (in days) to receive an alert: Title: Senior Facilities Engineer (Manufacturing) Requisition ID: 69452 Date: Apr 24, 2025 Location: Dublin, Leinster, IE Department: Maintenance Description: Job Summary Reporting to the Facilities Manager, the Senior Facilities Engineer will work with and support the site Facilities Team to ensure that the West Dublin facility is maintained to the highest cGMP standard. The Senior Facilities Engineer will play a key role in the specification and procurement of plant and facility equipment and will contribute to ongoing and future site and building development projects. Essential Duties and Responsibilities Report to the Facilities Manager. Analyse and investigate general facilities/maintenance issues, preparing and compiling written reports for the Facilities Manager with solutions and recommendations. Ensure HVAC, compressors, chilled water and general site services are operating to the required cGMP standards. Assist with the installation and set-up of new production cells and services to include validation in conjunction with Quality. Work closely with the HSE Manager to identify and address all health, safety and environmental issues on the site. Management of facility maintenance systems to in-house quality compliance standards i.e. Quality Systems ISO 9001/ISO 13485 and Environmental Management Systems ISO 14001 & OHSAS 18001. Liaise with the Quality/Compliance Department with respect to room/facility qualifications and required documentation. Support and participate in Quality Risk Assessments with respect to facility design and qualification. Actively participate and comply with all West HSE programs and regulations. Maintain a neat and orderly work environment in accordance with West 6S program. Other duties as assigned. Education Degree (Level 8) in Facilities or Mechanical Engineering or related discipline. Additional Trades Qualification is an advantage. Work Experience Minimum of 10 years working within a high-volume manufacturing environment. Additional Requirements While performing the duties of this job, the employee is regularly required to, sit, stand, walk, talk, hear, see and use hands and finger to operate office equipment (ie phones, computers, copies, etc.). Sitting and/or standing for extended periods may occur as well as getting to and from offices and building sites. The ability to be able to lift and carry various items up to 40 pounds. The employee is occasionally exposed to wet and/or humid conditions and fumes or airborne particles. The employee occasionally works near moving mechanical parts and or equipment. The noise level in the office work environment is usually quiet. The noise level in the manufacturing work environment is moderate to loud. Hearing protection is required at all times in the manufacturing work environment. Job requires mental skill or ability such as communication, decision making (sometimes quick), interpreting data, reading or writing, organization, problem solving, understand direction, supervise and speak publicly, etc. Preferred Knowledge, Skills and Abilities In depth knowledge of plant systems preferably in the pharmaceutical/medical device industry. Proven experience in the qualification, operation and maintenance of Grade C (or higher) cleanrooms. Working knowledge of AHU/HVAC, chilled water, compressed air, dryers and electrical systems. Ability to read electrical, hydraulic and pneumatic schematic diagrams/P&IDs. Proficient in asset management ensuring maintenance of the validated state of plant and equipment. Experience of working in an EU GMP controlled environment. Experience in cold storage facility maintenance and drug handling is essential. Ability to negotiate annual SLA's for plant critical equipment and support systems. Act as site SME for site CMMS and equipment uptime. Act as the point of contact for vendors and contractors. Must be familiar with computers and various software programs. Familiarity with SAP, Master Control or similar systems and databases, a plus. Excellent communication and interpersonal skills. Good analytical skills. Ability to work both independently with little direction, and as a member of a team. Ability to manage several projects at once to meet established timelines is essential. Some understanding of the injection moulding process is desired. Travel Requirements 5%: Up to 13 business days per year Physical Requirements Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects. #J-18808-Ljbffr
Select how often (in days) to receive an alert: Requisition ID: 70671 Date: Jul 31, 2025 Location: Dublin, Leinster, IE Description: At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary Note: This is a Fixed-Term contract until June 2026 In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications. Essential Duties and Responsibilities Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety. Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures. Ensure technical and customer requirements for assigned projects are achieved. Develop and maintain required validation and project management documents. Conduct or participate in routine project reviews with Project Teams and Management Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts. Develop and/or review engineering change requests for modifications to processes, equipment and facilities. Troubleshoot and repair of all automation. Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation. Ensure automation lines are meeting their targeted output and OEE by analyzing production data. Maintain quality finished product through proper maintenance and operation of all automation. Provide timely notification to shift leaders and program managers of maintenance and down time issues. Interfaces daily with engineering manager and shift support staff. Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules. Performs other duties as assigned by management. Exhibits regular, reliable, punctual and predictable attendance. Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management. Education Associate's Degree In a relevant Engineering subject required or Bachelor's Degree In a relevant Engineering subject preferred Work Experience Minimum 3 years Experience in medical device industry or other regulated industry required Minimum 3 years Experience in supporting technical project management preferred Preferred Knowledge, Skills and Abilities Background in medical devices/pharmaceutical would be a plus. Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards Travel Requirements 5%: Up to 13 business days per year Physical Requirements Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects. Additional Requirements Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues. Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in orderto apply to West, please send an email to Apply.Accommodation@westpharma.com . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening. #J-18808-Ljbffr
Select how often (in days) to receive an alert: Title: Manager, Sourcing Requisition ID: 71748 Date: Oct 28, 2025 Location: Dublin, Leinster, IE Department: Procurement Description: At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life‑saving and life‑enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary In this role, you will lead and manage category and sourcing oversight and sourcing roadmap activities for your assigned sourcing lead across key category / sub‑category areas. The scope of this role reaches across all global categories for all West operating units supporting sourcing strategy, planning and process delivery across early‑to‑late stage supply chains, includes alternate and second sourcing within development and commercial areas for direct materials, capital assets and indirect sourcing as apply. The role includes sourcing process expertise, project management, planning, Stakeholder and Supplier Relationship Management and Strategic Portfolio Management as applies to meet enterprise and business requirements. Essential Duties and Responsibilities Lead implementation and project manage ALL sourcing initiatives and events for assigned category(s) and any boarder Opex procurement operations as directed – includes MvB, EOI, RFx, etc. Review, assess and evaluate sourcing proposals and business case within Strategic Sourcing Category leads and across Operating unit partners and implement sourcing strategy, process and tactically deploy plans, methodology and reporting Support any contract negotiations and oversight with an emphasis on financial, commercial terms and conditions, risk management, compliance and business continuity while supporting business escalation and issue resolution, as applies Lead and support business partners to develop and enforce compliance to sourcing framework by managing supplier and service per West Strategic Sourcing Category Management, Sourcing Process and Operating Model Project manage and support business function partners on sourcing and procurement policies, procedures and business process through stakeholder management, team interactions and defined training programs, performance metrics, as applies Develop, implement, and improve project management operating models, structured methodology, tool kit consistent with industry project management principles and best‑practice including reporting to enhance sourcing process and improve category performance and supply risk issues, as required Introduce new and innovative ideas for the sourcing and procurement of materials, goods, and services utilizing best‑practice project management approaches Within assigned category sourcing events, actively partner and support Supplier Relationship (SRM) and team were engaging with existing suppliers and service providers as part of Global Strategic Sourcing Team overall Education Bachelor's Degree in procurement, business, supply chain or related scientific or technological qualification or equivalent experience required Master's Degree in related fields preferred Project management qualified preferred Work Experience Minimum 7 years in procurement, sourcing and project management role required Experience in category management, sourcing, technical transfer and sourcing projects across development to commercial in direct material and indirect sourcing Extensive knowledge and understanding of sourcing process, direct material and indirect sourcing market, environment across pharma, device and biotech industry areas Demonstrated ability to globally source, deliver project and influence stakeholder engagements in delivery of technical sourcing strategy, planning and events Preferred Knowledge, Skills and Abilities Ability to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description Ability to always comply with the company’s safety and quality policies License and Certifications Program and Project Management\Certified Project Management Professional (PMP)-PMI Upon Hire preferred Manufacturing\Lean Six Sigma Certification-IASSC or Agile Upon Hire preferred Additional Requirements Experience in key sourcing, procurement, and project experience in GMP Pharma, Medical Device with demonstrated experience in delivery of MvB, EOI, RFx events, projects and related methods and process for Direct and / or Indirect Category Areas as well as Procurement Opex tactical sourcing projects preferred Service and issue orientated, ability to work within teams or independently and to deadlines Adaptable to a multicultural environment, valuing diversity within a virtual global team environment Excellent project management and organizational skills with strong experience and knowledge of sourcing process Position operates in a professional office environment. Read, analyze and interpret technical and financial data, information and documents Observe and interpret situations, analyze and solve problems Strong Excel, PM Toolkit and report development skills. Strong analytical skills and business acumen. Ability to assess opportunities in the business and apply supply chain related solutions. Ability to make independent and sound judgment #LI-JJ1#LI-HYBRID Travel Requirements 20%: Up to 52 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre‑employment drug screening. #J-18808-Ljbffr
Select how often (in days) to receive an alert: Title: Director, Sourcing Requisition ID: 71672 Date: Oct 28, 2025 Location: Dublin, Leinster, IE Department: Procurement Description This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. No relocation is provided for this opportunity. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life‑saving and life‑enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary In this role, you will lead procurement efforts for a global category and sub‑categories. This role is responsible for creating, developing, implementing, and sustaining category strategy, strategic sourcing plans and roadmap that directly supports of business and operating unit objectives and displays professional/ethical business practices. Drive cross‑functional consistency of the globally harmonized procurement operating model and category management framework and strategic sourcing responsibilities and processes, while establishing and implementing best practices across key business and stakeholder engagements. Partner with the operation units, business stakeholders, Procurement pillars and the other key stakeholders to plan and decide what activities and delivery within cross‑functional teams and to collaborate on product compliance and supply assurance. Act as the business and functional communicator to convert and tactically deliver upon enterprise targets into procurement and sourcing deliverables. Essential Duties and Responsibilities Lead procurement and sourcing leads to be successful delivering their objectives and provide mid‑to‑long term direction and vision across accountable categories managed. Lead and influence management structures as to balance priorities and process improvement in regard of meeting structure and rigor, use of guidance playbook frameworks, policy documents as applies to provide necessary flexibility and agility in responding to short‑medium‑long term business demands. Guide and support the sourcing teams to apply globally harmonized category management framework and processes and execute sourcing, contracting initiatives to deliver optimal total cost of ownership, consolidate supplier base and drive efficiency through the chosen solutions, together with a multitude of global stakeholders at various levels and locations, leveraging scale and scope across the internal manufacturing network. Provide proactive management SRM and SPM for supplier base, and manage supply issues, performance and innovation for tiered classification of supplier. Inform and coordinate communication with Global Supply Chain leads on supplier issues with recommendations for resolution. Understand and have excellent category and sourcing knowledge of Direct Materials, Capital Assets and Indirect Sourcing landscapes, supply and service markets for goods and services in terms of supplier bases, technologies, competitive environment, market trends and cost drivers. Key advantage to have device, electrical, electronics and moulded component knowledge including scientific injection and compression moulding experience for wearable, containment and administration system products. Find and implement strategic sourcing solutions previously unknown to West, or previously known but not actioned. Make necessary organizational structure changes to meet goals and objectives. Recommend best practice standards and internal policies globally, and vet them with leadership on suitability to be implemented on a global level. Identify and assess risks and benefits of sourcing decisions and clearly present proposals to mitigate risks collaboratively, ensuring sustained product supply‑quality‑compliance. Build and keep up a trustful and fruitful relationship with cross functional peers. Align cross functional targets as to balance resources. Perform supplier relationship management to ensure continuous improvement and innovation, best in class pricing, product and service quality, continuity of goods and services, and alignment with internal stakeholders and company strategies. Conform with and abide by all regulations, policies, work procedures, instructions, and all safety rules. Ensure adequate protection of confidential information and documentation. Restrict access to confidential information. Ensure that key operational and essential documentation files are properly stored. Education Bachelor’s Degree Business or related technical degree or equivalent experience required Master’s Degree MBA preferred Work Experience Minimum 10 years progressive business experience in sourcing / supplier / category management or related functions required Medical device manufacturing experience preferred Preferred Knowledge, Skills and Abilities Able to be aware of all relevant standard operating procedures and company policy as they are related to the position covered by this Job Description Excellent Category Management, Sourcing, SRM, SPM and Contracting - lead negotiation experience Demonstrated leadership in line management, high‑performing teams with ability to influence Demonstrated ability to manage projects using project management process, tools and techniques Broad procurement and sourcing knowledge with Direct Materials, Capital Asset and Indirect Sourcing markets Ability to partner and work with senior leadership teams at manufacturing sites and global functions Excellent influencing, change management, and negotiation skills. Present and advocate sourcing cases to a variety of audiences with self‑confidence. Ability to respectfully communicate to and challenge senior leadership. Openness for new initiatives, fast learner, proactive. Track record of leading teams and building effective working relationships both internally and externally. Excellent presentation, communication, and interpersonal skills. Results orientation. Excellent analytical capabilities. Self‑starter and independent worker. Proficiency in English. #LI-JJ1 #LI-HYBRID Travel Requirements 20%: Up to 52 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre‑employment drug screening. #J-18808-Ljbffr
