IT Project Manager|Kneat Implementation at Osprey Life Sciences IT Project Manager|Kneat Implementation at Osprey Life Sciences in Milton Village, Massachusetts Posted in about 11 hours ago.

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full-time IT Project Manager-Kneat Implementation A World Class Company Osprey Life Sciences, LLC is a leading consulting and services firm specializing in providing comprehensive technology solutions for Life Sciences IT organizations. Our primary focus is on assisting these organizations in effectively and efficiently delivering solutions that support their business objectives and their mission to enhance human health and improve lives. Overview Osprey Life Sciences is partnering with a growing biotechnology client to identify an experienced IT Project Manager to lead the implementation of a digital validation platform, with Kneat experience strongly preferred (ValGenesis or comparable platforms also considered). This role will drive a high-impact GMP initiative supporting the organization's evolution from Research & Discovery into Clinical Development and Commercial Manufacturing. The ideal candidate is a collaborative, results-driven project leader with experience managing regulated software implementations, engaging cross-functional stakeholders across Quality, Validation, Manufacturing, Regulatory, and IT, and successfully delivering complex projects from initiation through deployment in a fast-paced Life Sciences environment. Key Responsibilities Project Leadership & Execution Lead the end-to-end implementation of a digital validation platform, including planning, execution, validation, deployment, and operational transition. Develop comprehensive project plans, implementation roadmaps, resource strategies, budgets, timelines, and risk mitigation plans. Proactively manage project risks, issues, dependencies, and competing priorities while ensuring successful project delivery. Coordinate project governance, status reporting, executive communications, and steering committee updates. Ensure projects are delivered on schedule while maintaining compliance with GMP and organizational quality standards. Stakeholder & Change Management Partner with Quality, Validation, Manufacturing, Regulatory Affairs, IT, and business stakeholders to align project objectives and implementation strategy. Facilitate cross-functional meetings, decision-making sessions, and executive communications. Build consensus among technical and business teams while managing evolving priorities in a fast-paced environment. Drive organizational change management and support user adoption throughout implementation. GMP, Validation & SDLC Partner with Quality and Validation teams to define validation strategy, documentation, testing, and compliance requirements. Lead project activities supporting requirements gathering, business process analysis, governance, validation planning, and implementation. Ensure adherence to GMP, CSV/CSA, SDLC, and validation lifecycle methodologies. Support inspection-ready documentation, traceability, risk assessments, and compliance deliverables. Required Qualifications Minimum 5 years of IT Project Management experience leading enterprise software implementations. Proven experience implementing Kneat or a comparable digital validation platform such as ValGenesis. Experience managing GMP-regulated software implementations within biotechnology, pharmaceutical, or Life Sciences organizations. Strong understanding of Computer System Validation (CSV), Computer Software Assurance (CSA), validation lifecycle management, and regulated SDLC methodologies. Demonstrated success leading medium-to-large cross-functional programs involving Quality, Validation, Manufacturing, Regulatory Affairs, and IT. Experience developing project plans, governance structures, resource strategies, budgets, and executive communications. Excellent stakeholder management, facilitation, negotiation, and communication skills. Ability to thrive in fast-paced, highly regulated environments while balancing strategic objectives with hands-on project execution. Preferred Qualifications Experience supporting organizations transitioning from Research & Discovery into Clinical Development and Commercial Manufacturing. Experience leading digital transformation or enterprise Quality initiatives. PMP certification or equivalent Project Management certification. Experience within growing biotechnology organizations undergoing increased regulatory maturity. We offer an excellent compensation and benefits package with challenge and opportunity to learn, grow, and contribute to a stimulating, fast-paced environment. Osprey Life Sciences is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status,