Senior Program Manager, Biologics GMP Projects

Plainsvc; Oklahoma City (OK); On-site; USD 90,000 - 130,000; Full time

Job summary

Plainsvc is seeking a Senior Program Manager to lead complex biologics development and manufacturing projects within a CDMO environment. You will own planning, delivery against contracted commitments, and coordination with clients, regulatory teams, and cross-functional groups.

The ideal candidate has 3+ years leading people and 5+ years in project/program management in regulated pharma/biotech or aerospace settings, with strong communication and strategic thinking to drive results.

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, or related field; advanced degree and/or PMP certification is a plus.
• 3+ years in people leadership and 5+ years in project/program management in regulated pharmaceutical, biotechnology or aerospace environments.
• Knowledge of biologics processes, cGMP manufacturing, supply chain, and regulatory requirements; Lean and process improvement experience.

Responsibilities

• Lead process development and/or GMP manufacturing projects with end-to-end oversight, managing all phases to meet timelines, budget, quality and regulatory standards.
• Establish and maintain strong client relationships with proactive engagement and clear communication throughout the project cycle.
• Coordinate with process development, manufacturing, QA, regulatory, supply chain and vendors to align project deliverables and finances.

Skills

Leadership

Project management

Communication

Lean/process improvement

Education

Bachelor's degree in Life Sciences or Engineering

PMP certification

Tools

MS Project

Smartsheet

Job description

Plainsvc is seeking a Senior Program Manager to lead complex biologics development and manufacturing projects within a CDMO environment. You will own planning, delivery against contracted commitments, and coordination with clients, regulatory teams, and cross-functional groups.

The ideal candidate has 3+ years leading people and 5+ years in project/program management in regulated pharma/biotech or aerospace settings, with strong communication and strategic thinking to drive results.