Valspec2mo ago

CQV Validation Engineer - Recent Graduates

Non-Headquartersmid

Engineering

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Quick Summary

Key Responsibilities

Support CQV activities for GMP manufacturing and utility equipment,

Technical Tools

Engineering

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

We are seeking a motivated and detail-oriented Entry-Level Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for GMP manufacturing and utility equipment at a client site. This role is ideal for a recent engineering or life sciences graduate who is interested in gaining hands-on experience in pharmaceutical and biotechnology manufacturing environments. The Equipment Validation Engineer will work as part of a collaborative CQV team and will receive structured training and mentorship from experienced validation professionals. This position offers exposure to GMP equipment systems, regulatory compliance, and real-world validation execution in a client-facing setting.

Responsibilities

~1 min read

→Support CQV activities for GMP manufacturing and utility equipment, including:
→
- →Autoclaves
- →CIP/SIP systems
- →Bioreactors
- →Incubators
- →Freezers and refrigerators
- →Centrifuges
- →Washers
- →Controlled temperature units
- →Environmental chambers
- →HVAC systems
- →Clean steam generators
- →WFI systems
- →Process tanks
- →Utility systems (compressed air, nitrogen, etc.)
→Assist in the development, execution, and documentation of validation deliverables, including:
- →User Requirements Specifications (URS)
- →Design Qualification (DQ)
- →Installation Qualification (IQ)
- →Operational Qualification (OQ)
- →Performance Qualification (PQ)
- →Qualification summary reports
→Execute protocol testing under the guidance of senior CQV engineers and accurately document results.
→Participate in commissioning activities and assist with troubleshooting equipment issues during startup and qualification.
→Support equipment risk assessments and impact analyses as part of validation planning.
→Collaborate with Engineering, Automation, Manufacturing, and Quality teams to support project execution.
→Maintain compliance with cGMP, FDA, and internal quality standards.
→Communicate test results, observations, and issues clearly to project team members.

Requirements

~1 min read

Bachelor’s degree in engineering, Life Sciences, or a related technical discipline (recent graduates encouraged to apply).
0–2 years of experience in a regulated manufacturing or validation environment (internship, co-op, or academic project experience acceptable).
Interest in pharmaceutical, biotechnology, or life sciences manufacturing.
Basic understanding of GMP concepts and validation principles preferred.
Exposure to IQ, OQ, and PQ activities is a plus but not required.
Familiarity with manufacturing equipment, utilities, or automated systems is beneficial.
Strong attention to detail, technical writing ability, and willingness to learn.
Ability to work on-site and collaborate effectively in a team-based environment.