Job Description Help for Job Description. Opens a new window. Overview Project Manager to act as the central point of contact for a cross-functional, multi-site risk-assessment program. The role keeps activities aligned across products, sites and functions, and manages the logistics and cadence that hold the program together.

Key Responsibilities:

• Coordinate confirmatory-testing logistics, including retained-sample selection, shipment to laboratories, and coordination with manufacturing sites, stability centres and testing labs.
• Manage program timelines, actions and meeting cadence, including preparation and follow-up across the core cross-functional team.
• Serve as the interface point between technical/documentation, site, analytical, quality and regulatory functions.
• Maintain trackers and status reporting for leadership visibility. Required skills & experience
• Project management or PMO experience, ideally in a GMP pharmaceutical setting.
• Strong stakeholder-management and cross-functional communication skills.
• Familiarity with GMP logistics (samples, stability, lab coordination).
• Highly organized, proactive, and comfortable managing multiple workstreams.

EOE Statement:

Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. To find out more about Real, please visit www.realstaffing.com