Engineer II, Validation

Grow in Greenville, NC; Greenville (NC); On-site; USD 85,000 - 100,000; Full time

Job summary

Thermo Fisher Scientific in Greenville, NC is seeking a Talent Engineer II, Validation. You will join a global team and contribute to validation activities ensuring compliance, quality, and operational excellence across facilities in pharmaceutical manufacturing, lab operations, and quality control.

You will apply IQ/OQ/PQ protocols, manage validation projects independently, and work with automation systems. Strong technical writing, risk assessment, and communication skills are essential.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Chemistry, or related technical field.
• 2 years of validation experience in a GMP/regulated environment preferred.
• 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.

Responsibilities

• Conduct validation activities to ensure compliance and quality across facilities.
• Support GMP/regulatory compliance in pharmaceutical manufacturing and labs.
• Collaborate with cross-functional teams on validation projects and documentation.
• Maintain quality systems and ensure timely completion of validation milestones.

Skills

cGMP knowledge

FDA regulations

Technical writing

Risk assessment

Data analysis

Communication

Project management

Metrology

Education

Bachelor's degree in Engineering or Life Sciences

Advanced degree preferred

Tools

Automation systems

Computer system validation

Microsoft Office

Job description

Talent Engineer II, Validation

Thermo Fisher Scientific

Greenville, NC, USA

• Full-time

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.

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

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.)

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