Junior Validation Engineer: GMP Compliance & Documentation

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

Benefits offered by this job

Onsite role

Contract-to-hire

Job summary

Actalent is seeking an Equipment Validation Engineer to support validation activities, author documentation, and assist with change control within a GMP-regulated manufacturing environment. The role blends office-based documentation with hands-on exposure to manufacturing operations, based in Columbus, OH.

Responsibilities include validating equipment, maintaining protocols, and collaborating with engineering and manufacturing teams to ensure adherence to GMP standards.

Qualifications

• 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.

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

Skills

Validation

Protocols

CPP

CQA

SOP

Education

Bachelor's degree in Engineering or Life Sciences

Job description

Actalent is seeking an Equipment Validation Engineer to support validation activities, author documentation, and assist with change control within a GMP-regulated manufacturing environment. The role blends office-based documentation with hands-on exposure to manufacturing operations, based in Columbus, OH.

Responsibilities include validating equipment, maintaining protocols, and collaborating with engineering and manufacturing teams to ensure adherence to GMP standards.