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CQV Engineer (Facilities, Utilities, and Equipment)
CQV Engineer (Facilities, Utilities, and Equipment)Automated Systems, Inc. • Tampa, FL, US
CQV Engineer (Facilities, Utilities, and Equipment)

CQV Engineer (Facilities, Utilities, and Equipment)

Automated Systems, Inc. • Tampa, FL, US
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Overview

CQV Engineer (Facilities, Utilities, and Equipment)

Contract, 6 months | Automated Systems, Inc. | United States

Posted On 09 / 05 / 2025

Job Information

Pharma / Biotech / Clinical Research

$48 - $60

State / Province : Florida

City : Tampa

33634

Job Description

CQV Engineer - Facilities, Utilities, and Equipment

Location : Tampa, FL - Onsite. Contract Duration : 6+ months, potential for extensions. Compensation : $48 – $60 per hour (based on experience).

Automated Systems, Inc. is seeking a CQV Engineer to take on a contract role with one of our pharmaceutical manufacturing clients located in Tampa, FL. In this role, you will be providing commissioning, qualification, and validation support across facilities, utilities, and equipment within this expanding operation.

Job Role Summary

Our client is expanding and requalifying its Tampa, FL facility, which supports the development and commercialization of innovative oral solid drug products. The site includes new product development suites (with powder-in-capsule / powder-in-bottle micro-dosing capabilities), state-of-the-art manufacturing areas for tablets and highly potent compounds, and modern packaging suites with product serialization capabilities.

Responsibilities

  • Author and execute commissioning and qualification protocols (IQ / OQ / PQ).
  • Support lifecycle documentation for facilities, utilities, and process equipment.
  • Partner with operations, engineering, and quality teams to ensure compliance with cGMP and regulatory expectations.
  • Lead troubleshooting, deviation investigations, and corrective action development.
  • Maintain validation project schedules and deliverables to meet regulatory and business needs.

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or related discipline.
  • 5+ years of CQV experience in pharmaceutical / biotech environments.
  • Strong knowledge of FDA, cGMP, and ASTM E2500.
  • Experience with oral solid dosage (OSD) products or high-potency manufacturing is a plus.
  • Excellent communication, documentation, and organizational skills.
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