Position Description

Bachelor’s degree in engineering, science, or similar. Candidate must have a minimum of 5-8 years of experience with qualification, protocol generation and execution in FDA-regulated companies. Responsibilities will require performing manufacturing process and equipment qualification activities for a global oral solid dosage pharmaceutical company.

Key Skills:
• Knowledge and understanding of Pharmaceutical GxPs and excellent GMP documentation skills
• Must be high energy, self-directed and driven, and must be able to work independently or with little supervision with sense of urgency accomplishing each task assigned
• Ability to effectively interact with individuals at all levels
• Intermediate to advanced MS Word and Excel needed as well as TrackWise, SharePoint, and PDF creator software experience
• Excellent written and verbal communication skills