Commissioning, Qualification & Validation Engineer

Commissioning, Qualification & Validation Engineer


Job ID: 10168102

Muskegon, MI, US

Engineering

Associate Degree

Full Time, Temporary

$55 - $65/hr

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Muskegon, MI, US

$55 - $65/hr

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Engineering

Associate Degree

First Shift (Day)

Job details

Commissioning, Qualification & Validation Specialist

 

  • Location: 100% onsite, Muskegon, Michigan (49445)

  • Shift: Office hours; site core hours 9:00 AM–2:00 PM, most work 8:00 AM–5:00 PM

  • Type: W2 contract (C2C OR THIRD PARTY arrangements will NOT be considered)

  • Pay Rate: Negotiable – Up to $55 – $65/hour based on DIRECT related experience

  • Contract Duration: Estimated to end: 8/30/2026 (Contract extension possibilities)

  • Work Authorization: Must be currently located and authorized to work in the United States without CURRENT sponsorship transfer requirements

 

Key Responsibilities:

  • Execute commissioning, qualification, and validation of equipment in construction projects for the pharmaceutical industry or their suppliers

  • Prepare and execute protocols and reports for installation and operational qualification (IQ/OQ)

  • Communicate and coordinate validation activities with various departments and personnel

  • Oversee and review validation area processes and procedures

  • Inspect equipment and define work, materials, and labor required

  • Coordinate schedules for multiple projects and workstream leaders

  • Translate engineering direction into actionable plans for site and third-party contractors

  • Manage project schedules and third-party contractor execution

  • Write vendor scope documents for engineering and service work

  • Ensure solutions and documentation meet safety, quality, and code requirements

 

Requirements:

  • Associate or bachelor’s degree in engineering, construction management, or related field

  • Experience in chemical or pharmaceutical manufacturing, including FDA Good Manufacturing Practices and OSHA CFR 1910.119 (process safety management for highly hazardous chemicals)

  • Familiarity with mechanical, electrical, and instrumentation systems

  • Strong organizational and planning skills

  • Expereince with life science and chemical industry manufacturing practices

 

Work Authorization: Must be currently located and authorized to work in the United States without CURRENT sponsorship transfer requirements. - No C2C or third-party candidates.~

 

*** Kelly does not expense relocation/interview costs. ***

 

Important information: To be immediately considered, please send an updated version of your resume to Deas172@kellyservices.com.

 

10168102

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