Job description

New Opportunity in Morrisville, NC working for a leading organization focusing on customizable and innovative solutions for analytical progress, experimental to marketable sterile and oral solid manufacturing, packaging, microbiology, cGMP biostorage, environmental monitoring, and pharmaceutical support.

You will accountable for results in a fast-paced environment and is responsible for production of drug products for delivery and clinical trials. You will operate the manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). Responsible for employing acceptable techniques while working in manufacturing environments and demonstrating proficiency in all department procedures, and mentoring new technicians, by providing work instruction and overseeing assignments.

Essential Functions

Manufacturing Technologies for Sterile Liquids:

Education and Experience

**This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**