Facilities/Utilities/HVAC Lead

Pharmatek Consulting • New Brunswick, NJ

2d

About The Position

We are looking for a CQV Lead with expertise in production equipment such as isolators, bioreactors, fume hoods, BSCs, and TCUs. The candidate will be responsible for protocol development and execution to ensure production equipment meets operational and regulatory standards.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• 10+ years of experience in validating production equipment in pharmaceutical environments.
• Expertise in isolators, bioreactors, fume hoods, and other lab equipment.
• Strong knowledge of regulatory requirements and risk -based validation approaches.
• Excellent project management and problem -solving skills.

Responsibilities

• Develop and execute commissioning, qualification, and validation protocols for production equipment.
• Coordinate with equipment vendors for FAT/SAT activities and ensure integration into facility systems.
• Oversee equipment calibration, performance verification, and documentation.
• Lead risk assessments to identify and mitigate potential equipment compliance risks.
• Provide cross -functional support for other CQV efforts within the project.

What This Job Offers

• Career Level: Mid Level