Conduct analytical research and validate/transfer methods to test pharmaceutical products for conformance to established specifications.

Perform analytical testing on R&D batches and associated stability studies and generate analysis report with minimal supervision.

Perform analysis on Cleaning Validation samples and generate analysis report.

Maintains confidentiality.

Possesses sound documentation skills.

Demonstrates ability to prioritize conflicting demands.

Executes assigned tasks within established schedule.

Writes and speaks clearly and concisely.

Develop & maintain expertise through continuing education & training.

Comply with Company policies, procedures, rules and regulations.

Competency with Microsoft Office Suite.

Strong organizational skills, attention to detail and ability to multi-task.

Must understand GMP regulations.

Bachelor's Degree or Master's Degree in Chemistry or Pharmaceutics.

Two years of pharmaceutical work experience is required with a Master's degree.

Five years of pharmaceutical work experience is required with a Bachelor's degree.

Must have HPLC, GC, Dissolution, UV experience.