Process Improvement Lead

NO C2C - W2 Only!R&D Process Improvement LeadSector: Biopharmaceuticals / R&DWe are seeking an R&D Process Improvement Lead to drive operational excellence across our global Research& Development organization. In this role, you will act as a strategic partner to Business Process Owners (BPOs) and Subject Matter Experts (SMEs), authoring the SOPs and Work Instructions that safeguard our quality and compliance standards.Strategic Authoring: Collaborate with cross-functional stakeholders (Pharmacovigilance, Regulatory Affairs, Clinical Operations) to draft, revise, and harmonize R&D-owned process documents (SOPs, WIs).Continuous Improvement: Drive process improvement initiatives by identifying gaps, providing document guidance, and promoting best practices across functional areas.Visual Workflows: Create detailed process maps using Microsoft Visio to ensure clarity and consistency in global R&D operations.Compliance & Audit Readiness: Support periodic document reviews, manage change controls within the EDMS, and ensure the organization remains in a state of inspection/audit readiness.Learning & Development: Support the creation of training materials and quizzes, potentially serving as a Training Coordinator to ensure seamless implementation of new processes.Must Haves:Education: Bachelor's degree in a scientific, clinical, or process-oriented field.Experience: 5+ years of experience within a Biopharmaceutical R&D organization, with a demonstrated track record in process improvement and document authoring.Technical Savvy: Proficiency in Microsoft Visio and extensive experience working within an Electronic Document Management System (EDMS)Subject Matter Expertise: Solid understanding of GxP regulations and the ability to operate effectively in a fast-paced, changing environment.Soft Skills: Exceptional negotiation and networking skills, with a systematic approach to problem-solving and a meticulous attention to detail.