C&Q Specialist - Clean Room Validation | Florida Onsite

ProQuality Network; Tampa (FL); On-site; USD 55,000 - 103,000; Part time

Job summary

ProQuality Network is currently seeking a Validation Support Contractor in Florida. The role focuses on hands-on C&Q activities within clean rooms and regulated manufacturing environments, including CTUs, incubators, equipment and utilities.

You will develop and execute qualification protocols, review documentation, and ensure traceability across projects. The ideal candidate will perform SAT, IQ/OQ/PQ and SMEPAC activities, collaborate with Engineering, Quality, Manufacturing, Microbiology, and

Qualifications

• Extensive hands-on C&Q experience in regulated manufacturing environments.
• Experience executing qualification protocols for CTUs, clean rooms, incubators, equipment, and utilities.
• Ability to develop and execute validation protocols, reports and traceability documentation.
• Collaborates with Engineering, Quality, Manufacturing, Microbiology, vendors, and contractors.

Responsibilities

• Execute SAT, IQ/OQ/PQ, SMEPAC, containment, room, equipment, CTU, and utility qualifications.
• Develop and execute validation protocols, reports, and traceability documentation.
• Perform C&Q activities for clean rooms, incubators, CTUs, equipment, and utilities.
• Support projects involving an encapsulator, high-potent suite, misting booth, DHU, iCAPS, BMS, compressed air, and auxiliary equipment.
• Support incubator conversion from walk-in incubator to freezer and qualification of a pharmaceutical filling room and associated utilities for new equipment.
• Perform documentation review, troubleshooting, and SOP support.
• Collaborate with Engineering, Quality, Manufacturing, Microbiology, vendors, and contractors.

Skills

C&Q / CQV Validation

IQ/OQ/PQ

Documentation skills

Fast-paced environment

Team collaboration

Job description

ProQuality Network is currently seeking a Validation Support Contractor in Florida. The role focuses on hands-on C&Q activities within clean rooms and regulated manufacturing environments, including CTUs, incubators, equipment and utilities.

You will develop and execute qualification protocols, review documentation, and ensure traceability across projects. The ideal candidate will perform SAT, IQ/OQ/PQ and SMEPAC activities, collaborate with Engineering, Quality, Manufacturing, Microbiology, and