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ThermoFisher Scientific

Engineer II, Validation

Greenville, NC, United States

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Job details

Posting language: English
Posted: Sep 6, 2026

Original job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join our collaborative team as a Validation Engineer II at Thermo Fisher Scientific, where you'll contribute to global healthcare and scientific advancement. In this role, you'll be responsible for ensuring compliance, quality, and operational excellence across our facilities through comprehensive validation activities. Working with advanced technologies and diverse teams, you'll help maintain high standards in pharmaceutical manufacturing, laboratory operations, and quality control.

REQUIREMENTS:

Bachelor's degree in Engineering, Life Sciences, Chemistry, or related technical field. Advanced degree preferred
2 years of validation experience in a GMP/regulated environment preferred but not required.
Experience with IQ/OQ/PQ protocols and execution
Experience managing validation projects independently
Experience with automation systems and computer system validation
Experience with quality management systems and documentation

Knowledge, Skills, Abilities:

Comprehensive knowledge of cGMP, FDA regulations, and industry standards (ISO, GAMP5)
Strong technical writing skills for validation documentation
Proficiency in risk assessment and gap analysis
Strong data analysis and problem-solving capabilities
Clear verbal and written communication skills
Proficient in Microsoft Office applications
Knowledge of calibration and metrology principles
Ability to work in cleanroom environments when required
Effective interpersonal skills for team collaboration
Ability to manage multiple projects
Knowledge of statistical analysis and process control methods
Consistent record of completing projects on schedule in a deadline-oriented environment

Note: We are not able to provide relocation assistance or visa sponsorship for this role.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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More about this job

Skills

Good manufacturing practices
Microsoft Office
Personal protective equipment
Regulatory compliance
Pharmaceutical processes
Quality control
SAP IQ
Quality assurance procedures
Documentation
Technical writing
Hazard assessment
Data analysis
Problem solving
Communication skills
Interpersonal skills
Collaboration
Statistics
Control engineering

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