Validation Engineer, cGMP Systems & Automation

biotech; Columbus (OH); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental, and Vision benefits

401(k) matching

Education Assistance

Job summary

PSC Biotech in Columbus, Ohio, seeks a Validation Engineer to oversee system validation activities in regulated manufacturing. Responsibilities include supporting validation lifecycles, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.

The ideal candidate should have a Bachelor's degree, at least 3 years of experience in computerized system validation, and familiarity with cGMP requirements. The offer includes comprehensive health benefits and a supportive work environment.

Qualifications

• Minimum of 3 years of experience in computerized system validation.
• Strong knowledge of cGMP requirements and validation frameworks.
• Experience with validation documentation including protocol development.

Responsibilities

• Support the validation lifecycle for automation and computerized systems.
• Partner with Engineering, Quality, and IT to ensure regulatory compliance.
• Assist in configuration, testing, and troubleshooting of software applications.

Skills

Computerized system validation

Technical troubleshooting

Cognitive skills

Cross-functional collaboration

Education

Bachelor’s degree in Engineering or related discipline

Job description

PSC Biotech in Columbus, Ohio, seeks a Validation Engineer to oversee system validation activities in regulated manufacturing. Responsibilities include supporting validation lifecycles, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.

The ideal candidate should have a Bachelor's degree, at least 3 years of experience in computerized system validation, and familiarity with cGMP requirements. The offer includes comprehensive health benefits and a supportive work environment.