Cell Therapy Project Manager

SOKOL GxP Services is a leading provider of GxP compliance, CQV/validation, and workforce solutions for life sciences manufacturing and quality operations. As a Cell Therapy Project Manager, you will play a pivotal role in driving continuous improvement initiatives within the Cell Therapy Global Quality team, ensuring projects are executed efficiently and in alignment with industry standards.

Key responsibilities include:

Leading continuous improvement projects within the Cell Therapy Global Quality team; Scheduling and managing meetings, documenting minutes, and maintaining project dashboards and documentation (charter, milestones, risk log); Managing internal steering meetings and coordinating cross-functional activities with internal support teams; Engaging subject matter experts for change management and process impact discussions; Managing projects end-to-end, from initiation through closure, to meet contract obligations and charter deliverables; Running project governance processes including kickoff, status, and executive sponsor meetings, as well as reporting and risk/issue tracking; Managing resources to achieve deliverables and coordinating stakeholder communications; Planning, executing, controlling, and closing projects to meet scope, schedule, budget, and quality objectives using GPS standards and methodologies; Supporting the execution of change management strategies, defining change metrics, and measuring effectiveness; Identifying and analyzing stakeholders, delivering engagement activities, and ensuring leadership alignment; Developing and delivering communications strategies, messaging, and conducting pulse checks and surveys.

Requirements Required Qualifications:

Bachelor's degree in arts, sciences, or engineering; 8+ years of project management experience in a regulated or validated environment (life sciences manufacturing/quality context); Experience managing end-to-end projects, including scope, schedule, budget, and risk/issue tracking; Proficiency with formal project management tools/platforms for managing plans, milestones, and status reporting; Proficiency maintaining structured project documentation (project charter, milestones, risk log) using documentation and reporting tools; Experience coordinating cross-functional teams and subject matter experts to deliver project outcomes; Experience running project governance with senior leadership (steering committee and executive sponsor meetings).

Preferred Qualifications:

PMP certification; Experience with cell therapy or biopharmaceutical manufacturing projects; Strong organizational, critical thinking, and decision-making skills; Proven ability to proactively identify, document, resolve, or escalate risks and issues; Track record of holding teams accountable for on-time deliverables. Benefits H ealth insurance, holiday pay, 401(k) program, referral program , and other benefits Hourly rate, $: 80.7 - 85.7 12-month contract with possible extension

Job Type:

Hybrid (min 50% on-site required) Working hours: regular business hours.

Rotating shift:

1 week - Tue/Thur onsite, 2 week - Tue/Wed/Thur onsite.