Junior Validation Engineer - GMP Compliance (Onsite)

Actalent; Columbus (OH); On-site; USD 40,000 - 56,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

HSA

Job summary

Actalent in Columbus, OH is seeking a Validation Engineer to support equipment validation, author validation docs, and collaborate with manufacturing and engineering to ensure GMP compliance.

This contract-to-hire role blends office-based documentation with hands-on manufacturing exposure, requiring 0-2 years experience, a technical degree, and strong communication.

The position is fully onsite in Columbus with competitive hourly pay and benefits; apply by Sep 28, 2026.

Qualifications

• Knowledge of validation protocols, process validation, and validation testing.
• Experience with equipment validation, CPP, CQA, risk assessment, SOP, and work instructions.
• Bachelor's degree in Engineering, Life Sciences, or related technical field OR equivalent pharmaceutical manufacturing experience.
• 0-2 years of professional experience.
• Strong written and verbal communication skills.
• Ability to work independently and take ownership of responsibilities.
• Strong organizational and problem-solving abilities.
• Demonstrated initiative and willingness to learn in a regulated environment.
• Familiarity with GMP, pharmaceutical, and engineering technical documentation.

Responsibilities

• Support equipment validation activities for manufacturing equipment and systems.
• Author, revise, and maintain validation protocols and documentation.
• Execute validation activities and ensure compliance with procedures.
• Support change control processes related to equipment modifications and maintenance.
• Update SOPs, work instructions, and operational procedures.
• Collaborate with engineering and manufacturing during installations and modifications.
• Provide validation support for equipment changes and system improvements.
• Assist with continuous improvement initiatives in manufacturing operations.
• Ensure GMP compliance and validation standards.
• Participate in investigations, risk assessments, and reviews as required.
• Monitor CPPs and CQAs related to validated processes.

Skills

Validation knowledge

SOP documentation

CPP/CQA awareness

Communication skills

Independence

Education

Bachelor's degree in Engineering, Life Sciences, or related technical field

Job description

Actalent in Columbus, OH is seeking a Validation Engineer to support equipment validation, author validation docs, and collaborate with manufacturing and engineering to ensure GMP compliance.

This contract-to-hire role blends office-based documentation with hands-on manufacturing exposure, requiring 0-2 years experience, a technical degree, and strong communication.

The position is fully onsite in Columbus with competitive hourly pay and benefits; apply by Sep 28, 2026.