Biopharmaceutical - CQV PROJECT DIRECTOR

MMR Consulting

$110K — $150K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • 12+ years of biotech project management experience in cGMP environments
  • Experience managing capital projects is essential
  • Background in Greenfield project execution required
  • Strong leadership and initiative skills for complex, multi-stakeholder projects
  • Mentorship abilities to support junior team members' development
  • Basic AutoCAD proficiency
  • Degree in Mechanical, Chemical, Electrical or related field; Project Management certification is a plus

Responsibilities

  • Provide technical guidance for project assessments, design, and commissioning of facilities
  • Prepare comprehensive business cases detailing project purpose, risks, and budgets
  • Oversee design firms, vendors, and stakeholders for project execution
  • Manage all phases of Capital Projects from feasibility to completion
  • Review and approve technical documents such as specifications and datasheets
  • Ensure safety integration in all projects through comprehensive reviews
  • Support project management tools for tracking and documentation
  • Facilitate cross-departmental meetings to enhance project progress

Benefits

  • Opportunity to work with a specialized and growing team
  • Engagement with a variety of industry stakeholders
  • Project diversity including both upgrades and Greenfield projects
  • Chance to travel and collaborate on-site across multiple U.S. facilities
  • Potential for involvement in business development and industry representation opportunities
Full Job Description
Previous Pharmaceutical/Biotech experience is mandatory for this role.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning and qualification, of equipment, systems and facilities.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work will require working out of client's facilities.

The work will require working on-site at client's facilities, which are located in US. Travel is required to US is required.

Responsibilities
  • Provide technical guidance into the assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
  • Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
  • Manage other design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
  • Manage Capital Projects
  • 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

  • Review and approve 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 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.


Qualifications

  • 12+ years of experience in the biotech industry in 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.
  • Previous Greenfield 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.
  • Degree, preferably in Mechanical, Chemical, Electrical or other industry related discipline.
  • Certification in Project Management would be an asset.
  • Travel may be required on occasion. Ability to travel to the US would be an asset.


Salary range: 110,000$ -150,000$ based on experience.

Similar Jobs

More Jobs at MMR Consulting

More Pharmaceuticals & Biotech Jobs

Find similar Biopharmaceutical - CQV PROJECT DIRECTOR jobs: