Technical Project Manager (Assembly)

QCS Staffing Ltd; North Carolina; On-site; USD 110,000 - 140,000; Full time

Job summary

QCS Staffing Ltd seeks an experienced Technical Project Manager for an Assembly project based in North Carolina. The role covers end-to-end oversight from design through IOQ, coordinating third-party partners and challenging schedules to ensure milestones are achieved.

The position requires extensive pharma/biotech project background, large capital project leadership, and strong contractor management capabilities, supporting a landmark US facility initiative.

Qualifications

• Extensive pharmaceutical or biotech project experience.
• Significant drug product manufacturing experience.
• Experience overseeing large capital projects.
• Client-side, owner-side or EPCM leadership experience.
• Strong contractor management experience.

Responsibilities

• Act as client-side owner for Assembly.
• Provide end-to-end oversight from detailed design through IOQ completion.
• Manage and coordinate third-party execution partners.
• Challenge contractor schedules, resource plans and delivery assumptions.
• Track project scope, risks, schedule and milestone achievement.
• Coordinate alignment between Engineering, MSAT, Operations, Quality, CQV and Construction.

Skills

Pharma/Biotech PM

Capital project leadership

Contractor management

Client-side ownership

Schedule & risk management

Job description

Technical Project Manager (Assembly) – US, North Carolina – Initial 12-Month Contract – Life Sciences

Support a landmark project as QCS partner with a global biologics organization to drive delivery of a cutting-edge facility in North Carolina. Be part of a large-scale investment and play a pivotal part in bringing this world-class program to life.

Our client is seeking an experienced Technical Project Manager to support the delivery of their project based in North Carolina on an initial 12-month contract.

What You’ll Deliver

• Act as client-side owner for Assembly
• Provide end-to-end oversight from detailed design through IOQ completion.
• Manage and coordinate third-party execution partners.
• Challenge contractor schedules, resource plans and delivery assumptions.
• Track project scope, risks, schedule and milestone achievement.
• Coordinate alignment between Engineering, MSAT, Operations, Quality, CQV and Construction.

Experience required:

• Extensive pharmaceutical or biotech project experience
• Significant drug product manufacturing experience
• Experience overseeing large capital projects
• Client-side, owner-side or EPCM leadership experience
• Strong contractor management experience