Biopharmaceutical - CQV Lead/ PROJECT MANAGER

MMR Consulting

• $110K — $130K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 10+ years in the biotech industry focusing on project management for equipment and facilities, particularly in cGMP operations.
  • Hands-on experience with capital projects and Greenfield projects is essential.
  • Demonstrated leadership and initiative in managing complex, multi-departmental projects.
  • Proven mentorship abilities to develop junior and intermediate team members.
  • Basic proficiency in AutoCAD is beneficial.
  • Bachelor's degree in Mechanical, Chemical, Electrical or relevant discipline is required.
  • Project Management certification is a plus.

Responsibilities

  • Provide technical guidance for assessments, design, project management, commissioning, and start-up of client facilities and processes.
  • Lead project execution from feasibility to completion, involving all stages such as design and procurement.
  • Prepare comprehensive business cases detailing project purpose, risks, budget, and schedule.
  • Manage collaborations with design firms, equipment vendors, and construction stakeholders.
  • Review technical documents like P&IDs and project specifications to ensure compliance and technical accuracy.
  • Integrate safety protocols throughout the project lifecycle, including HAZOP reviews and engagement with EHS representatives.
  • Coordinate with cross-functional departments to enhance project execution and facilitate decision-making.

Benefits

  • Opportunity to work in a growing team within the biotech sector, focusing on innovative projects.
  • Involvement with diverse projects ranging from facility upgrades to new installations.
  • Potential for professional development through mentorship responsibilities.
  • Exposure to varied aspects of project management and client relations, enhancing career growth opportunities.
  • Engagement in client-facing sessions, including presentations at industry conferences.
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 out of the client's facilities in Raleigh, North Carolina.

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.
  • 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 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 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.


Qualifications

  • 10+ 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.

Similar Jobs

More Jobs at MMR Consulting

More Pharmaceuticals & Biotech Jobs

Find similar Biopharmaceutical - CQV Lead/ PROJECT MANAGER jobs: