CQV Project Manager

Stark Pharma Solutions Inc; New England (ND); On-site; USD 120,000 - 180,000; Full time

Job summary

Stark Pharma Solutions Inc. in the New England region seeks a CQV Project Manager to lead commissioning, qualification, and validation programs for pharmaceutical and biotech facilities.

You will steer cross‑functional CQV activities, manage scope, schedules, and client expectations to ensure compliant, on‑time project delivery. The role requires strong leadership, excellent communication, and proven ability to collaborate with clients, engineering teams, and stakeholders throughout the project

Qualifications

• Experience leading Commissioning, Qualification, and Validation (CQV) projects.
• Proven ability to manage project scope, schedules, and client expectations.
• Experience collaborating with clients, engineering teams, and cross-functional stakeholders.
• Strong project management and leadership skills.
• Excellent communication and stakeholder management abilities.
• Experience supporting pharmaceutical or biotechnology manufacturing projects is preferred.

Responsibilities

• Lead CQV programs from planning through execution.
• Manage project scope, schedules, and client expectations.
• Partner with clients, engineering teams, and project stakeholders.
• Drive project delivery while meeting quality and compliance objectives.
• Lead cross-functional CQV activities throughout the project lifecycle.
• Support the successful delivery of biotech and pharmaceutical manufacturing facilities.
• Coordinate with internal and external teams to ensure project success.
• Maintain effective communication with clients and stakeholders throughout project execution.

Skills

CQV Management

Project Management

Stakeholder Management

Communication

Leadership

Job description

Position: CQV Project Manager

Location: New England Region

Duration: Long Term

Job Overview

We are seeking a CQV Project Manager to lead Commissioning, Qualification, and Validation (CQV) programs for pharmaceutical and biotechnology manufacturing projects. In this role, you will lead cross‑functional CQV activities, manage project scope, schedules, and client expectations, while driving successful project delivery, quality, and compliance. This is an excellent opportunity to work on state‑of‑the‑art biotech and pharmaceutical manufacturing facilities.

Key Responsibilities

• Lead CQV programs from planning through execution.
• Manage project scope, schedules, and client expectations.
• Partner with clients, engineering teams, and project stakeholders.
• Drive project delivery while meeting quality and compliance objectives.
• Lead cross‑functional CQV activities throughout the project lifecycle.
• Support the successful delivery of biotech and pharmaceutical manufacturing facilities.
• Coordinate with internal and external teams to ensure project success.
• Maintain effective communication with clients and stakeholders throughout project execution.

Required Qualifications

• Experience leading Commissioning, Qualification, and Validation (CQV) projects.
• Proven ability to manage project scope, schedules, and client expectations.
• Experience collaborating with clients, engineering teams, and cross‑functional stakeholders.
• Strong project management and leadership skills.
• Excellent communication and stakeholder management abilities.
• Ability to drive project delivery while maintaining quality and compliance objectives.
• Experience supporting pharmaceutical or biotechnology manufacturing projects is preferred.