Specialist II, Supply Chain

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit RESILIENCE is a first-of-its-kind manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption. Founded in 2020, the company is building a sustainable network of high-tech, end-to-end manufacturing solutions to ensure the medicines of today and tomorrow can be made quickly, safely, and at scale. RESILIENCE will offer the highest quality and regulatory capabilities, and flexible and adaptive facilities to serve partners of all sizes. By continuously advancing the science of biopharmaceutical manufacturing and development, RESILIENCE frees partners to focus on the discoveries that improve patients’ lives. Core Responsibilities Provide primary support and coordination for packaging documentation changes, including packaging artwork changes and Bill of Material (BOM) change form completion. Project manage packaging documentation changes from initial notification through implementation, ensuring sufficient time is available to implement the change to the timescales requested by the customer. This includes understanding market expectations and communicating throughout the site so that QA and Planning remain aligned. Create Operations Change Management (OCM) and Veeva records and appropriate Action Items to support the creation of new components and changes to existing components. Hold and participate in routine Job Tracking communication meetings with key assigned customers as needed, and maintain Job Tracking information for assigned jobs, including a forward view of upcoming changes. Maintain artwork within the appropriate artwork management systems and ensure approved documentation is transferred to approved vendors and suppliers as needed. Manage the use of external artwork resources as appropriate. Send artwork samples as required to the appropriate representative per MIF. Systems & Master Data Set up and progress projects within Gazelle for Artwork Order Requests (AOR), Technical Labeling Request Forms (TLRF), and Labeling Request Forms (LRF) for packaging documentation changes. Initiate and maintain the SAP Master Data Governance (MDG) system for globally planned materials for the West Chester site. Coordinate SAP and D365 transactions required to create new components to ensure timely implementation. Serve as the site's SAP super user and support the site with ERP master data queries. Support the site with ERP (SAP/D365) access requests. Collaboration & Continuous Improvement Support cross-site initiatives to standardize workflows and align processes with internal and external customers. Participate in inter-departmental and inter-company project teams, representing packaging, documentation and master data requirements. Interface with appropriate Marketing, Operations, Project Management, Quality Assurance, and Development personnel. Create and update supporting documentation for specific job functions. Support various site-driven projects and market launches. Minimum Qualifications Experience in one or more of the following areas: packaging operations, production planning, quality assurance, IQC packaging technical services, or MRP and advanced planning systems. Working knowledge of packaging processes, artwork processes, compliance issues, and cGMPs. Knowledge of cGMP and FDA regulations involving data management and validation requirements. Detailed knowledge of SAP, Material Resource Planning (MRP), and advanced planning systems related to pharmaceutical production processes. Good interpersonal and project management and coordination skills. Analytical, assertive, highly disciplined, and independent, with demonstrated high-level attention to detail and the ability to prioritize competing work with minimum supervision. Preferred Qualifications Bachelor's degree, preferably in a technical or scientific field, with knowledge of MRP and planning related to pharmaceutical production processes. 3+ years of experience in packaging documentation, artwork management, supply chain or a related function with a cGMP-regulated environment. Experience with change management (Veeva or Track wise). Proven ability to work independently and professionally in a cGMP-regulated environment. Knowledge of inventory control and document management systems. Physical & Work Environment Work is performed onsite at the West Chester supply site in a combined office and cGMP manufacturing environment. Requires periodic access to packaging and production areas, including gowning and adherence to area-specific requirements where applicable. Requires extended periods of computer-based work reviewing artwork, master data, and change documentation. Occasional business travel may be required to support cross-site initiatives and supplier coordination. Work Schedule 8 hours – Monday–Friday, onsite at the West Chester site. The work schedule listed reflects the employee's expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, including a request to work overtime, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments. Sponsorship or Support for Work Authorization Sponsorship or support for work authorization, including visas, is not available for this position. Equal Employment Opportunity Employer Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $60,000.00 - $93,750.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. #J-18808-Ljbffr Resilience