Senior Validation Engineer - Pharma OSD & Packaging

Grow in Greenville, NC; Greenville (NC); On-site; USD 90,000 - 130,000; Full time

Job summary

Thermo Fisher Scientific in Greenville, NC, is seeking a Validation Engineer III to lead manufacturing process validation for Oral Solid Dose (OSD) and packaging. You will write and execute IQ/OQ/PQ protocols, analyze data, and prepare reports supporting regulatory compliance while collaborating with Manufacturing, Quality, and Technical Operations teams.

The role offers a balance of documentation and hands-on manufacturing support, with 70% desk-based work and 30% floor activity, and occasional

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Chemistry, or technical field.
• 5+ years of validation experience in regulated manufacturing environments.

Responsibilities

• Lead validation activities for Oral Solid Dose (OSD) and packaging processes.
• Develop, execute, and document IQ/OQ/PQ protocols.
• Analyze validation data and prepare technical reports for regulatory compliance.
• Support AVI validation activities as needed and collaborate with cross-functional teams.

Skills

Validation engineering

Good Manufacturing Practices

Analytical skills

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Thermo Fisher Scientific in Greenville, NC, is seeking a Validation Engineer III to lead manufacturing process validation for Oral Solid Dose (OSD) and packaging. You will write and execute IQ/OQ/PQ protocols, analyze data, and prepare reports supporting regulatory compliance while collaborating with Manufacturing, Quality, and Technical Operations teams.

The role offers a balance of documentation and hands-on manufacturing support, with 70% desk-based work and 30% floor activity, and occasional