Senior Project Manager – CDMO Pharma Manufacturing (Hybrid)

ADP, Inc.

West Saint Paul (MN)

Hybrid

USD 90,000 - 120,000

Full time

6 days ago
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Job summary

LTS Lohmann Therapy Systems in West St. Paul, MN is seeking a Senior Project Manager to lead complex development and commercial programs from initiation through closeout in a GMP pharmaceutical environment.

In this hybrid role, you will partner with internal teams and external customers, manage schedules and budgets, and ensure quality and compliance while guiding cross-functional teams to timely, on-scope delivery. Schedule: Mon-Fri, 8:00 AM–4:30 PM.

Qualifications

  • Bachelor's degree in engineering or related field required.
  • 5+ years of project management experience in pharma/GMP/CDMO.
  • Proven ability to lead cross-functional programs.
  • Strong ability to communicate complex topics to varied audiences.

Responsibilities

  • Lead senior-level project management activities across program lifecycle.
  • Manage complex customer-facing programs with timelines, scope, quality, risk, and cost.
  • Serve as a trusted contact for development and commercial programs with clear communication.
  • Communicate status, risks, decisions, and next steps to stakeholders.
  • Influence and lead cross-functional teams to align priorities and deliverables.
  • Apply PM methodologies and tools: timelines, agendas, risk tracking, logs.
  • Identify critical path activities and elevate significant risks.
  • Resolve issues involving SOWs, billing, materials, and scope changes.
  • Coordinate with accounting, supply chain, and ERP needs.
  • Facilitate phase-gate reviews, audits, and project meetings.

Skills

Project management
Cross-functional leadership
Stakeholder communication
Risk management

Education

Bachelor’s degree in engineering or related field

Tools

MS Project
SAP ERP
Microsoft Office

Job description

LTS Lohmann Therapy Systems in West St. Paul, MN is seeking a Senior Project Manager to lead complex development and commercial programs from initiation through closeout in a GMP pharmaceutical environment.

In this hybrid role, you will partner with internal teams and external customers, manage schedules and budgets, and ensure quality and compliance while guiding cross-functional teams to timely, on-scope delivery. Schedule: Mon-Fri, 8:00 AM–4:30 PM.

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