Validation Engineer

This role is located in North Augusta, South Carolina. Relocation is required. Apply now to learn more about our relocation assistance.

• Complete new asset and computer system validations.
• Validation Planning
• Commissioning and Qualification Protocol Drafting and Execution
• Validation Reporting
• Provide project updates to stakeholders and facilities management.
• Assist in the writing of facilities CAPAs and Deviations.
• Assist in completing software compliance assessments.
• Edit and create validation and other facilities procedures as needed.

• Minimum Education:
  
  Bachelor’s degree in Life Science or Engineering Discipline
• Technical Writing Skills
• Proficiency in Microsoft Word and Microsoft Excel.
• Good communication and writing
• Must have basic understanding of CQV processes.
• Good project management skills.
• Must be able to work cross functionally with stakeholders, vendors, and staff to oversee the completion of asset validations.
• 2-3 years of pharmaceutical industry experience preferably in manufacturing or engineering.
• Previous experience in equipment/software validation or quality engineering is desired.

• Must be able to push, pull, squat, stand and walk throughout the day.
• Must be able to lift 40 lbs.
• Must be able to wear safety shoes & glasses throughout the day while in designated areas. (provided by the company)
• You must be cleared by a physician to wear a respirator throughout the day while in designated areas.
• You must be able to work in a chemical environment.