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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.