HumanEdge is hiring: Pharmaceutical Manufacturing Associate in Boonton

Opportunity Description

Our client, a rapidly expanding contract development and manufacturing organization (CDMO) in the orally inhaled and nasal drug product (OINDP) space is specifically focused on providing early phase clinical trial materials for its clients. We are seeking an enthusiastic learner to support the Manufacturing group with formulation development, process development, GMP manufacturing, as well as peripheral support activities.

Company Information

• Biopharma

Job Duties

• Execute formulation development protocols at the bench scale; preparing solutions and reagents for experimentation as required
• Manufacture drug product for early-phase clinical trials in a GMP environment; comfort using spray drying and other manufacturing equipment a plus.
• Follow written Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP) and good documentation practices.
• Follow safe laboratory practices
• Experience using various analytical equipment a plus (HPLC, Karl Fisher, Laser Diffraction PSD)

Education

• Bachelors in Chemistry or related field

Experience & Skills Required

• Entry Level, 1-3 years in a pharmaceutical environment preferred