West Pharmaceutical Services

Supply Chain

• Actively support the short and long-term supply planning activities for assigned focus suppliers.
• Plan and schedule all customer orders through the manufacturing areas.
• Supervise planning specialists and plant purchasing function.
• Monitor all inventory levels and maintain within established guidelines.
• Establish and maintain data integrity in West systems.

Supply Chain Planning Supervisor

Analyst

• Perform routine and non-routine product and packaging release testing including, but not limited to, bacterial endotoxin, bioburden, particulate, silicone etc.
• Perform routine testing to support the plant functions including, but not limited to environmental monitoring, water testing, personnel monitoring, etc.
• Perform incoming testing for materials, including growth promotion testing in culture media and incoming test for biological indicators.
• Perform microbial identification using the WID-MID software®.
• Review data when required.
• Participate in basic laboratory support functions, such as cleaning, preparing materials and glassware for testing.
• Provide support for validations, method transfer and/or project work.
• Assist in preparation of work instructions, SOPs, and qualification documentation.
• Provide support in internal and external audits.
• Participate (or assist) in identification, investigation (OOS’s) and resolution of problems in the lab.
• Apply required cGMP regulations, data integrity and internal procedures.
• Adhere to established laboratory safety procedures.
• Meet individual and departmental goals as required.
• Willing to work as a team member with self-motivation, adaptability, and a positive attitude to ensure continuous improvement relative to laboratory functions. As well as work independently using established methods and procedures.

Associate Analyst, Analytical Lab

QA Engineer

• Develop and manage a high-performing West Design Quality global team responsible for ensuring: Execution of defined business goals & objectives.
• QMS processes which facilitate development of product which comply to applicable international quality and regulatory requirements.
• Partner with other Global Design Quality and Global R&D leaders to deploy strategic platform product development approaches to product development.
• Partner with other Global Design Quality and Global leaders to deploy harmonized, compliant, and scalable QMS solutions across the enterprise.
• Oversee and provide direction to cross-functional teams on design control and QMS elements including but not limited to change control, training, CAPAs, issue reviews, audit findings, investigations, risk management activities, document control, configuration control, and quality agreements.
• Establish, trend, and review KPIs and metrics with cross-functional leaders to drive improvements to the applicable elements of the QMS.
• Provide support in the creation of, resourcing for, and enforcement of development agreements for West proprietary products in collaboration with commercial, product management, R&D, regulatory, and operations.

Senior Director, QA Design Quality & Risk Management

• Provide strategic and technical leadership for the Quality Engineering function within a regulated medical device manufacturing environment.
• Lead and mentor a team of Quality Engineers to ensure consistent delivery of high-quality products that meet or exceed customer expectations.
• Align Quality Engineering priorities with operational and business objectives to achieve strategic alignment.
• Develop strong cross-functional partnerships with Design Quality Engineering, R&D, Manufacturing, Operations, Corporate Quality, and Supply Chain teams to drive alignment and performance.
• Ensure Quality Systems are compliant with regulatory and company standards (ISO 13485, 21CFR, EU MDR).
• Drive continuous improvement initiatives through process optimization, data analytics, and adoption of quality tools and technologies.

Senior Manager, Quality Engineering

Engineer

• Lead engineering, management, plant operations and global team members while working with vendors to develop engineering specifications for new equipment
• Drive forward the standardization & harmonization of production equipment and associated documentation across the global network
• Analyze and evaluate existing systems and processes with Process Engineering
• Work independently and with vendors to understand root cause of failures
• Take the lead in systematic problem-solving activities for manufacturing plants
• Coordinate and/or execute all necessary GMP related validations and/or process engineering evaluations

Senior Engineer, Compounding & Dimensioning Equipment

Manager

• Understand requirements and intended use of packaging & delivery systems, analytical testing and data correlation related to the pharmaceutical market
• Develop and implement scientific strategies and thought leadership aligned with business objectives
• Establish communities of practice, advancing knowledge and exchanging best practices
• Provide scientific guidance to internal teams and contribute to strategic planning
• Translate complex science into business strategy
• Interpret and communicate scientific data to internal and external audiences
• Engage with external stakeholders including regulatory agencies and business partners
• Build and maintain relationships with key opinion leaders and external scientific experts
• Represent the company at standard setting organizations, scientific meetings, conferences, and industry events
• Attend scientific conferences and meetings to stay up to date on the latest research and advancements
• Leverage analytical thinking for problem-solving
• Conduct independent research to support various projects
• Stay current with industry standards and compliance requirements

Senior Manager, Scientific Affairs

• Contributing to the development and implementation of the validation engineering strategy
• Ensuring qualification and validation of equipment, facilities, utilities, automated systems, processes and cleaning procedures are in accordance to GMP and relevant guidelines
• Lead the validation effort for all Strategic Projects on site
• Develop Validation Plans to support Site Validation Master Plan
• Act as site subject matter expert on Cleaning Validation, Process Validation, Equipment Validation, Computer System Validation, Data Integrity and Facility Qualification
• Preparation, review and approval of qualification and/or validation documentation (specifications, protocols, reports etc.)
• Review and approval of third party generated protocols and reports
• Fosters and encourages shared learning’s across the organisation
• Chair, schedule and minute validation meetings
• Perform periodic reviews of systems in order to maintain validation status
• Develop and implement site validation strategy to meet customer and West needs
• Represent West at customer meetings to ensure that the needs of the business are met
• Assist with the training and development of personnel at all levels of West on new processes or systems introduced to the company
• Ensure that all procedures are in place to facilitate the introduction of new processes and equipment
• Lead and manage a high performing team to deliver the defined business goals and objectives.

Principal Process Validation Engineer

• The Senior Process Engineer Global SME Lining is a member of the West global engineering team
• This role is key to implementing new technology, developing and introducing process improvements, standards, life cycle management and validation in select process areas
• Support capital investments and contributing to addressing complex assignments
• Initiate, lead and coordinate lining related continuous process improvement projects on quality, service, HSE and cost within the standard known/approved process frame
• Collaborate closely with the global equipment engineering team for specifying and standardizing of new and existing equipment

Global Senior Process Engineer

Solutions Engineer

• Participate in and capture outcomes of workshops and interviews with Subject Matter Experts
• Maintain identified features, user stories, tasks, gaps, and the relationships between them within the transformation portfolio
• Develop and share reporting that articulates progress and realization of benefits from transformation initiatives
• Drive execution of activities necessary to achieve our organizational goals
• Other duties as assigned

Solution Architect, Payroll & Time

• Provide technical and administrative services in a highly complex and global environment
• Support tools and functions providing endpoint deployment maintenance and management
• Consult with the business using standard services and defines implementation concepts
• Actively provide 3rd level support for related to tools like Microsoft Endpoint Configuration Manager
• Collaborate with the regional and global D&T organization to maintain existing endpoint configuration services
• Participate in local, regional, and global D&T projects and support project execution

Senior Solutions Architect, SCCM Administrator

Engineering Manager

• Reporting to the Sr. Global Process Engineering Manager, this role is primarily responsible for supporting the Global Processing Injection Molding group
• Evaluate and implement new equipment through the commissioning, validation and involvement of process improvement projects across all CM sites.
• Support the harmonization of process/tooling principles, practices, and procedures across Global Process/Tooling Engineering group.
• Provide all pertinent validations of both tooling and process. Interacts with site Engineering / Customers on new projects or issues pertaining to the Injection Molding processes.
• Define strategy in support of long-term and intermediate goals within Global Process Engineering
• Develop scope of work, plan and manage for Injection Molding/Equipment Validation projects
• Use strong analytical skills to understand and implement customer/user needs, market requirements and other design inputs.
• Support CM Sales team in all new business quoting and gathering customer requirements relating to Process Engineering requirements.
• Identify, execute, and implement process improvement initiatives across the Global platform.
• Provide leadership/guidance on the installation and validation of new equipment/process development through SAT/IQ/OQ/PQ.
• Ensure that procedures and systems are in place to facilitate the introduction of new processes and equipment.
• Drive idea creation, development, bread boarding/prototyping, feasibility testing, etc.
• Lead and advise component material selection with a strong emphasis on polymer selection for injection molded parts.
• Hands-on engineering, such as reverse engineering, simple assembly and machining work.
• Provide continuity for the validation program for assigned plant or functional area by preparing technical documentation/presentations.
• Provide project leadership for materials/process related projects by coordinating efforts of the various departmental disciplines for successful completion according to plan and budget.
• Managing internal and external resources to meet the technical requirements of the project.
• Work with Tooling Design team to plan innovative technical approaches to design solutions.
• Identify, monitor status of results or projects. Leveraging internal and external resources to solving complex problems.
• Help execute specific strategies, tactics and action plans for the location, as part of the overall Delivery Systems/Innovation product development plan.

Process Engineering Manager

Software Engineer

• Manage the engineering team to ensure that all plant equipment is fit for purpose and the business can achieve its manufacturing requirements
• Managing the engineering team in accordance with company policies and procedures.
• Maintaining equipment and services by supervising and carrying out as required, planned maintenance, breakdown repair and improvements to all plant equipment.
• Ensuring that the monitoring of upgrades and replacements is carried out using appropriate project management tools and delivered to time, cost and quality.
• To manage capital, revenue and improvement projects to time cost and quality.
• Manage track and record work on the maintenance management system.
• Responsible for analysing and reporting department performance
• Manage and liaise with contractors
• Ensure legislative compliance with all aspects of work undertaken by the department.

Engineering Supervisor

• Manage/Administer West Pharma's portfolio of SAP & Non-SAP applications globally
• Expertise in Application Life Cycle Management like installation, upgrades, support packages, and daily maintenance
• Maintain the integrity of SAP & Non-SAP environments
• Provide technical support for SAP issues
• Perform system refreshes and migrations
• Adhere to SAP Basis on-call support

Solution Architect, SAP Basis

Accounts Payable

• Support all aspects of the accounts payable process
• Ensure timely and accurate processing of invoices and payments
• Maintain strong supplier relationships
• Collaborate with internal departments to resolve discrepancies

Specialist, Accounts Payable, T&E

Risk

• Work closely with the Director, Global Risk and Insurance to support West commercial insurance strategies worldwide
• Actively participate in all phases of property/casualty insurance placements
• Identify potential loss exposures and analyze appropriate risk finance techniques
• Market and place designated insurance policies
• Provide ongoing oversight and support for financial and claims administration duties as required
• Maintain strong working relationships with internal and external clients
• Support property/casualty insurance negotiations
• Assist with claims management and reporting
• Generate property & casualty certificates of insurance requests upon request