Cell Therapy Project Manager
SOKOL GxP Services, El Paso, TX, United States
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.
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 elevate risks and issues;
Track record of holding teams accountable for on-time deliverables.
Health 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.
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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.
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 elevate risks and issues;
Track record of holding teams accountable for on-time deliverables.
Health 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.
#J-18808-Ljbffr