Project Manager

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Project Manager Full Time Woodstock, IL, US 11 days ago Requisition ID: 1297 Salary Range: $80,000.00 To $100,000.00 Annually About the Role Woodstock Sterile Solutions is seeking a skilled and driven Project Manager to lead technical projects supporting new product development within our facility. This role is critical in managing drug development projects from feasibility through pre‑commercialization, as well as overseeing technical transfers and customer product qualifications. You will serve as the primary point of contact for clients while coordinating cross‑functional teams to deliver high‑quality results on time and within scope. Key Responsibilities Develop, manage, and maintain detailed project timelines using MS Project, including task planning, resource allocation, and deliverables tracking Lead projects through the full lifecycle, ensuring milestones and client commitments are met Coordinate internal teams and client stakeholders to drive project execution and communication Identify risks, anticipate delays, and implement mitigation strategies Maintain accurate project documentation, plans, and status reports Track deliverables, project health, and customer satisfaction metrics Facilitate internal and external project meetings, including agendas and follow‑ups Manage project‑related contracts and requests Serve as the primary liaison for customers, ensuring strong communication and relationship management Support revenue tracking and billing through business systems (e.g., JDE) Ensure compliance with quality systems, cGMP standards, and safety requirements Host customer visits and provide project updates to leadership Qualifications Education: Bachelor's degree in Chemistry, Pharmacy, Engineering, or related field (required) PMP certification (preferred) Experience: 5+ years of relevant experience in pharmaceutical development and project management Experience managing client‑facing projects strongly preferred Have worked in CDMO/CMO industry Deep understanding of cGMP standards and FDA/ICH regulatory guidelines Strong project management and organizational skills Excellent written and verbal communication abilities Proven ability to manage multiple projects and priorities simultaneously Strong analytical thinking and problem‑solving skills High attention to detail and documentation accuracy Ability to work independently and in cross‑functional teams Proficiency with business software tools (MS Office, project management systems, etc.) Knowledge of cGMP and pharmaceutical development processes Ability to perform risk assessments and drive proactive solutions Physical Requirements Regular sitting, standing, walking, and computer use Occasional lifting (up to 30 lbs.) and physical movement as needed Collaborative and team‑oriented culture Strong focus on customer satisfaction and quality #J-18808-Ljbffr Woodstock Sterile Solutions