<p>Piper Companies is seeking a Project Manager to join a growing organization within the pharmaceutical manufacturing industry for a long-term onsite contract opportunity based out of Ridgefield, NJ. The Project Manager will support sterile injectable programs within a CDMO environment, leading technology transfer and manufacturing readiness activities while partnering with both internal technical teams and external clients.</p> <p>Responsibilities of the Project Manager include:</p> <ul> <li>Lead cross-functional technology transfer initiatives for sterile injectable products from client onboarding through GMP manufacturing. </li><li>Develop, track, and manage integrated project plans, timelines, and deliverables across multiple active programs. </li><li>Coordinate closely with manufacturing, engineering, quality, and validation teams to support equipment readiness, scale-up, and launch activities. </li><li>Serve as the primary customer-facing contact, providing clear communication, milestone updates, and proactive risk management. </li><li>Ensure project execution aligns with cGMP standards, internal quality systems, and regulatory expectations. </li></ul> <p>Qualifications for the Project Manager include:</p> <ul> <li>Bachelor's degree in engineering, life sciences, chemistry, pharmacy, or a related scientific discipline. </li><li>5+ years of project management experience within pharmaceutical or biopharmaceutical manufacturing environments. </li><li>Direct experience supporting sterile injectable products and technology transfer activities. </li><li>Strong understanding of aseptic processing, sterile fill-finish operations, and GMP requirements. </li><li>Demonstrated ability to manage multiple stakeholders and priorities in a fast-paced CDMO setting. </li></ul> <p>Compensation for the Project Manager:</p> <p>Salary Range: $150,000-$165,000/year (USD)</p> <p>Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K</p> <p>This job opens for applications on 3/29/26. Applications for this job will be accepted for at least 30 days from the posting date.</p> <p>Keywords: project manager, project management, sterile injectables, CDMO, technology transfer, tech transfer, aseptic processing, sterile manufacturing, fill finish, GMP, pharmaceutical manufacturing, validation, PPQ, scale-up, client management, stakeholder communication, regulatory compliance, quality systems, manufacturing readiness, injectable drug products, cross-functional leadership, process transfer, lyophilization, packaging readiness, risk management, scheduling, budgeting, program management.</p> <p>#LI-MB1 #LI-ONSITE</p>