• Be able to articulate work related issues clearly and effectively to management and peers 

• Performs accurate routine chemical testing (FTIR, TLC, PM, UV-Vis) to meet departmental objectives. 

• Documents testing in compliance with Good Documentation Practices. 

• Updates and routes SOPs, MOAs, Specifications through Documentum as delegated by supervisor. 

• Maintains accurate records of all work performed with respect to a given project. Ensures documentation meets facility audit as well as cGMP or GLP requirements. 

• Manages work and time based on departmental priorities using own judgement and objective reasoning. 

• Performs good housekeeping practices and follows safety related policies. Makes recommendations. 

• Performs peer review of data to ensure compliance and accuracy. 

• Assumes additional responsibilities as assigned. 

REQUIREMENTS 

• Possess a B.S. in Chemistry, Biology or related physical science.
• Typically, 0-2 years of related experience in pharmaceutical industry. Background in HPLC and other analytical techniques (GC, AA, UV, TLC, and wet chemistry) desirable.
• Must be proficient in Microsoft Office (Word, Excel, PowerPoint).
• Must be flexible with continually changing projects and priorities. 
• The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.