Ph3Print Team Lead Overview /h3 /brpThe Global Clinical Supply (GCS) organization manages the end-to-end clinical supply for the company’s portfolio. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to clinical sites across more than 60 countries, in compliance with worldwide regulations, company policies and standard operating procedures. /p /br /brh3Print Team Lead Responsibilities /h3 /brul /brliEnsure each component or bulk material used in label production is properly identified, not expired and verified throughout processing and that it corresponds to the written information on the work order before proceeding to the next step. /li /brliPrint, inspect, proof and maintain accountability for clinical product labels. /li /brliMaintain label inventory, including the disposal of expired materials. /li /brliServe as a Qualified Trainer. /li /brliConduct periodic quality inspections during the printing process to ensure product integrity. /li /brliPrepare shipments of labels to external packaging sites. /li /brliReceive bulk labels from booklet manufacturing vendors. /li /brliParticipate in equipment‑related testing and upgrades. /li /brliEnsure team members perform tasks in accordance with GMP and batch record instructions. /li /brliInitiate and implement process improvements aimed at increasing quality, customer satisfaction and efficiency. /li /brliMonitor the production schedule on a weekly, monthly and quarterly basis while managing group headcount and employee utilization. /li /brliAdvance operational capabilities by identifying new opportunities, seeking input from key stakeholders and implementing ideas. /li /brliLead, promote, and support the use of innovation and technology in Label Production. /li /brliRegularly evaluate employee performance, conduct development discussions and complete year‑end performance reviews. /li /brliManage the team, including problem‑solving and proactive escalation to next‑level management when needed. /li /brliLead local and global label projects, including organizing meetings and delegating tasks. /li /brliAuthor, review and approve standard operating procedures and job aids for packaging and labelling activities. /li /brliParticipate in and support internal and external audits. /li /brliRecommend process improvements to enhance team efficiency. /li /brliCoordinate and train new employees. /li /br /ul /br /brh3Education /h3 /brul /brliBachelor’s degree or equivalent with four years of relevant experience. /li /brliHigh School Diploma or equivalent with six years of relevant experience in Pharmaceutical Operations, preferably in a clinical supply‑related area. /li /br /ul /br /brh3Preferred Experience and Skills /h3 /brul /brliAt least two years of experience in management or leadership positions. /li /brliMinimum of six years of relevant experience in supply chain or operations. /li /brliAbility to collaborate effectively across functional boundaries in multicultural environments to align stakeholders and drive tech transfer strategies and solutions. /li /brliDemonstrated problem‑solving ability, strong verbal and written communication skills and excellent interpersonal skills. /li /brliStrong understanding of clinical supplies and supply chain processes with relevant regulatory and GMP requirements. /li /brliAbility to establish clear goals, delegate effectively and hold self and others accountable. /li /brliAbility to succeed in a dynamic environment and adapt to changing priorities. /li /brliWell‑developed team facilitation and leadership skills, with the ability to build inclusive team environments. /li /brliProven project and team management skills. /li /brliPrior experience with SAP is beneficial. /li /br /ul /br /brh3Required Skills /h3 /brul /brliClinical Supply Chain Management /li /brliCross‑Functional Collaboration /li /brliCustomer Satisfaction /li /brliDriving Continuous Improvement /li /brliGMP Compliance /li /brliInventory Control Management /li /brliLogistics Management /li /brliMaster Batch Records /li /brliOperational Performance Management (PM) /li /brliOrganizational Optimzation /li /brliPharmaceutical Packaging /li /brliProcess Improvements /li /brliProduction Planning /li /brliProfessional Integrity /li /brliProject Leadership /li /brliQuality Oversight /li /brliQuality Standards /li /brliRecordkeeping /li /brliResults‑Oriented /li /brliSAP Consulting /li /brliSAP Enterprise Resource Planning (ERP) /li /brliSAP Support /li /brliStakeholder Collaboration /li /brliSupply Chain Metrics /li /br /ul /br /brpbEmployee Status: /b Regular /p /brpbRelocation: /b No relocation /p /brpbVISA Sponsorship: /b No /p /brpbTravel Requirements: /b 10% /p /brpbShift: /b Not Indicated /p /brpbValid Driving License: /b No /p /brpbHazardous Material(s): /b No /p /brpbJob Posting End Date: /b 06/13/2026 /p /brpbRequisition ID: /b R /p /p #J-18808-Ljbffr