CQV Engineer (No C2C or Sponsorship is available)

Technical Source; Lebanon (IN); On-site; USD 55,000 - 83,000; Full time

Job summary

A leading engineering recruitment firm is searching for a Validation Engineer to work with a pharmaceutical manufacturing client in the Greater Indianapolis Area. This role requires a Bachelor’s degree in engineering and over 3 years of validation experience, specifically with HVAC and Utilities systems. Responsibilities include developing protocols, conducting temperature mapping, and validating building automation systems. Excellent communication and documentation skills are necessary for this long-term, on-site position.

Qualifications

• 3+ years of validation experience in a pharmaceutical environment.
• Experience with cGMP documentation and the entire validation life cycle.
• Strong understanding of HVAC and utilities systems.
• Knowledge of KNEAT.

Responsibilities

• Develop/Execute protocols for HVAC/Utilities.
• Conduct temperature mapping.
• Assist with validating building automation systems.
• Utilize Paperless Validation Software.
• Complete Required Documentation.

Skills

Validation Experience

Knowledge of KNEAT

cGMP Documentation

Education

Bachelor's Degree in Engineering or Related Field

Tools

KNEAT

Job description

Technical Source is currently in search of a Validation Engineer for a pharmaceutical manufacturing client in the Greater Indianapolis Area. This is a long-term contract position that requires on-site work. The qualified candidate should have experience conducting the Commissioning, Qualification, and Validation of HVAC and Utilities Systems in a Pharmaceutical Environment.

Responsibilities of the Validation Engineer include:

• Develop/Execute Protocols for HVAC/Utilities
• Conduct Temperature Mapping
• Assist with Validating Building Automation Systems (Hardware)
• Utilize Paperless Validation Software
• Complete Required Documentation

Qualifications of the Validation Engineer include:

• Bachelor's Degree in Engineering or Related Field
• 3+ Years of Validation Experience
• Experience with cGMP documentation and the entire Validation Life Cycle
• Knowledge of KNEAT

*No C2C or Sponsorship is available at this time*

*Compensation will scale based on experience and fit*