Full-Time

Biopharmaceutical – Senior Project Manager

Posted on 9/9/2025

MMR Consulting

MMR Consulting

Compensation Overview

$70k - $120k/yr

Chicago, IL, USA

In Person

Projects require on-site work at client facilities; Bradley, IL area ~1.5 hours from Chicago.

Category
Business & Strategy (1)
Requirements
  • Previous Pharmaceutical/Biotech experience is mandatory for this role.
  • 10+ years of experience in engineering / project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
  • Previous PM capital projects experience is required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Basic knowledge of AutoCAD.
  • Engineering degree, preferably in Mechanical, Chemical, Electrical Engineering.
  • Certification in Project Management would be an asset.
  • Travel may be required on occasion. Ability to travel to the US would be an asset.
Responsibilities
  • Provide technical guidance into the engineering assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
  • Lead or support project execution from feasibility through to project completion/handover, including all project stages such as: Feasibility Assessments Concept Design, Basic Design, Detailed Design Procurement Construction / Installation Project Controls - Monitoring Commissioning & Qualification
  • Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
  • Manage other engineering design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
  • Manage Capital Projects
  • Review technical documentation such as P&IDs, specifications, layouts, manuals, datasheets.
  • Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
  • Prepare/review automation sequences, as required for Process Automation.
  • Engage and coordinate with other engineering disciplines and other cross-functional departments (Process, automation, building / facilities, procurement, construction management, commissioning, qualification & validation, manufacturing operations, EHS, quality & compliance).
  • Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
  • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification & validation phases.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Visit construction and installation sites, wear necessary safety PPE.
  • Supervise contractors during critical installations of process equipment and associated utilities.
  • Other duties as assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable.

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INACTIVE