Validation Engineer II - GMP & Compliance Specialist

Regulatory Jobs; Greenville (NC); On-site; USD 75,000 - 110,000; Full time

Job summary

Join Thermo Fisher Scientific as a Validation Engineer II. You will contribute to global healthcare and scientific advancement by ensuring compliance, quality, and operational excellence across facilities through validation activities in pharmaceutical manufacturing, lab operations, and quality control.

Work with advanced technologies and diverse teams to maintain high standards and deliver projects on schedule, while supporting GMP/regulatory requirements and ongoing process improvements.

Qualifications

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

Responsibilities

• Ensure compliance, quality, and operational excellence across facilities through comprehensive validation activities.

Skills

GMP knowledge

FDA regs

Validation

Quality docs

Data analysis

Communication

Project management

Education

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

Advanced degree preferred

Job description

Join Thermo Fisher Scientific as a Validation Engineer II. You will contribute to global healthcare and scientific advancement by ensuring compliance, quality, and operational excellence across facilities through validation activities in pharmaceutical manufacturing, lab operations, and quality control.

Work with advanced technologies and diverse teams to maintain high standards and deliver projects on schedule, while supporting GMP/regulatory requirements and ongoing process improvements.