Job Title

Requisition

Location

Additional Locations

Job Description

Job Description Summary

Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices.

ESSENTIAL FUNCTIONS:

cGMP Active Pharmaceutical Ingredient (API) manufacturing.

Conduct lab and pilot scale chemistry methods to synthesize and produce pharmaceuticals.

Maintain strict FDA and cGMP compliance.

Routinely and effectively maintain laboratory and supplies.

Be able to troubleshoot and resolve technical issues along with comprehensive knowledge of hand tools. Follow Six Sigma and Lean manufacturing methods for stream lining and quality production.

Handling waste, solvents, raw materials (some hazardous) and potent compounds with the appropriate procedures and personal protective equipment (PPE).

Education:

Minimum of a Bachelor's degree in Chemistry, Biology or other science degree.

Experience:

Minimum of one to three years' previous experience in development, manufacturing or analytical chemistry.

Skills/Qualifications:

Knowledge of cGMP and FDA regulations, have a fundamental understanding of chemistry involving synthesis and purification methods; knowledge of potent compounds; knowledge and proficiently use MS Office Suite (Word, EXCEL, PowerPoint).

Skills/Competencies:

This role requires the candidate to have strong ability to work in a team environment; must be able to assume responsibility for their work; must be a self-starter and motivated; be safety conscious; excellent written and verbal communication skills; demonstrated mechanical aptitude, organizational, and multitasking skills; a high attention to detail with excellent documentation and record keeping abilities; be able to learn on the fly; understanding of process flow; must be able to lift 50 lbs. Ability and willingness to work nights, weekends, holidays and rotating shifts.

Other Skills:

Able to analyze, prioritize and manage multiple tasks.