Biopharmaceutical CQV Lead / Project Manager

Job overview

The Biopharmaceutical CQV Lead / Project Manager role is onsite at client facilities in Raleigh, NC. Compensation is not specified. MMR Consulting specializes in pharmaceutical and biotechnology project management, process, automation, facilities, and equipment commissioning and qualification. The role leads or supports capital projects from feasibility through completion and handover, including design, procurement, construction, commissioning, and qualification. It coordinates technical teams, vendors, contractors, and client stakeholders to deliver facility and process upgrades, renovations, and expansions safely and effectively.

What you'll do

• Provide technical guidance for assessments, design, project management, commissioning, and start-up
• lead or support project execution from feasibility through handover
• prepare business cases
• manage design firms, vendors, contractors, and stakeholders
• manage capital projects
• review technical documentation
• integrate safety into project design and execution
• coordinate cross-functional departments and project controls
• supervise contractors during critical installations
• visit construction and installation sites.

What we're looking for

Skills & competencies

biopharmaceutical cqv lead

project manager

mmr consulting

raleigh nc

client facilities

pharmaceutical

biotechnology

commissioning and qualification

capital projects

greenfield projects

project execution

occasional travel

Work arrangement

• Weekend coverage required

Why this role

The posting requires prior pharmaceutical or biotechnology experience, capital-project management experience, and Greenfield project experience. Occasional travel and support during shutdowns or extended hours may be required.

About the employer

MMR Consulting is hiring for this role. Industry: Other Scientific and Technical Consulting Services. Sector: 54.