Chemist Jobs

About The Position

Requirements

• Bachelor’s degree in Chemistry or Biochemistry or equivalent.
• Minimum five (5) years of experience in pharmaceutical quality control in a cGMP environment.
• Hands on thorough knowledge of analytical testing and instrumentation specifically HPLC, GC, Residual Solvents, KF, solid state testing.
• Familiarity with GMP requirements/regulations.
• Excellent organizational and planning skills.
• Strong written, verbal, and interpersonal communication skills.
• High attention to detail.
• Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.

Responsibilities

• Perform testing on intermediates and final products to meet production/client timelines.
• Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
• Test reference standards and stability samples.
• Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms.
• Verify data with second quality team member as required.
• Maintain all records as required to maintain compliance.
• Assist in the preparation of new and revised documentation as required.
• Provide support in the maintenance and calibration of laboratory analytical instrumentation.
• Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
• Act as the primary QC contact for the Production team and/or Program Manager for any given project or synthetic step.
• Provide necessary training and guidance to newer employees on GMP issues and analytical issues.