Technical Source is currently in search of a Validation Engineer for our pharmaceutical manufacturing client in Western North Carolina. This is a long-term contract position that requires on-site work. There is a possibility of full-time conversion if internal headcount allows. The qualified candidate should have experience conducting Equipment Validation in a Pharmaceutical Environment.

Responsibilities of the Validation Engineer include:

• Validate Pharmaceutical Manufacturing Equipment
• Conduct Process Performance Qualifications
• Qualify Lab Equipment
• Complete Required Documentation

Qualifications of the Validation Engineer include:

• Bachelor's Degree in Engineering or Related Field
• 1-3 Years of Experience working in a Pharmaceutical Manufacturing Environment
• Experience with cGMP documentation and the entire Validation Life Cycle

*No C2C or Sponsorship is available at this time*

*Compensation will scale based on experience and fit*