Senior Validation Engineer - Pharma QC Systems Expert

USAntibiotics; Bristol (TN); On-site; USD 80,000 - 100,000; Full time

Job summary

A pharmaceutical manufacturing company in Bristol, TN is looking for a Senior Technical Operations Validation Specialist. You will be responsible for process validation across a variety of systems and equipment. The ideal candidate will have over 5 years of experience in the pharmaceutical industry, a strong background in validation protocols, and expertise in quality assurance practices. This full-time position offers an opportunity to work in a collaborative environment with a focus on compliance and data integrity.

Qualifications

• 5+ years of experience writing validation protocols in pharma manufacturing.
• Experience with CGMP and FDA regulated environments.
• Knowledge of solid oral dosage form manufacturing processes.

Responsibilities

• Create validation protocols for processes and equipment.
• Provide technical support for QC laboratories.
• Support risk assessments and technical documentation.

Skills

Technical writing for validation protocols

Data analysis skills

Strong computer skills

Education

BS/BA in a STEM field

MS or Ph.D. preferred

Tools

LIMS

SAP

Job description

A pharmaceutical manufacturing company in Bristol, TN is looking for a Senior Technical Operations Validation Specialist. You will be responsible for process validation across a variety of systems and equipment. The ideal candidate will have over 5 years of experience in the pharmaceutical industry, a strong background in validation protocols, and expertise in quality assurance practices. This full-time position offers an opportunity to work in a collaborative environment with a focus on compliance and data integrity.