- Responsible for the development and modification of pharmaceutical products within a GMP environment
- Supports all activities required to develop, optimize and scale-up immediate and control release products
- Researches and compiles pre-formulation data on the drugs and excipients
- Ensure that all master manufacturing documentation, batch documentation, and other related documents required through the duration of the project are made available when required
- Development and design of original formulations
- Conducts relevant patent searches on formulations
- Designs, issues and evaluates formulation trials to develop optimized formulae
- Ensures the optimum manufacture of initial pilot, stability, bio, and small-scale production batches
- Prepares Pharmaceutical Development Reports for submitted products
Education & Experience:
- Minimum 5 years in a related position
- Education: B.Sc. or Master’s minimum in science related field
Job Type: Full-time
Salary: $100,000.00-$140,000.00 per year
Benefits:
- Dental care
- Paid time off
- Tuition reimbursement
Flexible Language Requirement:
Schedule:
Supplemental pay types:
Work Location: In person
