Global Project Manager, Pharma Capital Projects (US)

Siegfried; Wilmington (DE); On-site; USD 150,000 - 200,000; Full time

Benefits offered by this job

Competitive bonus

Employee share matching

401(k) match

Medical, dental, vision

Life, sickness and accident insurance

Voluntary life insurance

Job summary

Siegfried invites an experienced Global Project Manager to lead capital investment projects within a CDMO environment. You will supervise full lifecycle delivery from FEL1 through close-out, coordinating with internal and external teams to ensure safe, timely, and cost-effective execution.

The role requires a Bachelor’s in Chemical/Mechanical Engineering, PMP (or PE), and 8–12 years in pharma/CDMO settings, with CQV and cGMP knowledge. Travel to sites will be involved.

Qualifications

• Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or a related life sciences field (or equivalent).
• PMP certification or PE license preferred.
• 8–12 years of experience in chemical/pharma CDMO environments, CQV and cGMP/ICH Q7A knowledge.
• Proven ability to manage a capital portfolio >$50M.
• Strong knowledge of API development and matrix management.

Responsibilities

• Provide leadership for definition, organization and execution of capital investment projects from FEL1 to close-out.
• Manage at least one EPCM relationship to ensure safety, timeliness and cost-effectiveness.
• Deliver US capital project plans, develop briefs, create execution packages, and ensure on-time, in-scope delivery within defined costs.
• Lead cross-functional teams and communicate with stakeholders across sites.

Skills

Project management

Leadership

Communication

Travel readiness

Education

Bachelor’s degree in Chemical/Mechanical Engineering

PMP certification

Job description

Siegfried invites an experienced Global Project Manager to lead capital investment projects within a CDMO environment. You will supervise full lifecycle delivery from FEL1 through close-out, coordinating with internal and external teams to ensure safe, timely, and cost-effective execution.

The role requires a Bachelor’s in Chemical/Mechanical Engineering, PMP (or PE), and 8–12 years in pharma/CDMO settings, with CQV and cGMP knowledge. Travel to sites will be involved.