Quality Control Chemist

Description:       

• Facilitate and maintain cGMP within the company and requirements per ISO standards.
• Follow and implement Quality related SOPs & policies of the company.
• Test in-process, finished product and stability samples by following approved protocols and specifications.
• Operate and calibrate HPLC, GC, FTIR, UV-Vis., pH meter, Viscometer, Analytical Balance, etc.
• Validate analytical methods. Develop, write and revise applicable controlled documents under supervision.
• Maintain log books for laboratory record, material control, label control and equipment usage for production and packaging operations.
• Receive, sample, test and release labels, components and raw materials, following approved specifications.
• Contemporaneously document daily activities, rigorously adhering to cGMP/GLP and company standards.
• Monitor and document control data for water system, stability charts and temperature control, etc.

Qualifications:           

• Bachelor’s or Master's degree in Chemistry, Chemical Engineering, Pharmaceutical Engineering or equivalent related scientific or engineering fields.
• Excellent computer and MS software skills and ability to learn, use, and otherwise adapt to job-specific software, as necessary.
• Strong problem-solving aptitude, communication (spoken and written English) and multi-tasking skills.
• Strong knowledge of general QC analytical concepts, practices, and procedure and/or willingness to learn.
• Proficient knowledge of regulatory standards and/or willingness to learn.