Quality Control Chemist - HPAPI Analytics

Piramal Pharma Limited; Riverview (MI); On-site; USD 65,000 - 75,000; Full time

Job summary

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan is seeking a qualified Quality Control Chemist I to join our QC team. The role focuses on analytical testing and supporting manufacturing through raw material testing, cleaning verifications, and data documentation.

The candidate should have a Bachelor's degree in Chemistry or Biochemistry and ideally one year of pharmaceutical QC experience, with familiarity in analytical testing and

Qualifications

• Bachelor's degree in Chemistry or Biochemistry or equivalent.
• One year of experience in pharmaceutical quality control or equivalent is preferred.
• Familiarity with analytical testing and instrumentation.

Responsibilities

• Support manufacturing operations through testing of raw materials and starting materials to meet production timelines.
• Perform cleaning verifications on multi-use equipment using approved methods.
• Test reference standards and stability samples.
• Document sample preparation, equipment setup, and test results in laboratory notebooks or test record forms and verify data with a second quality team member.
• Assist in testing intermediates and final products to meet client requirements.
• Maintain QC laboratory and calibration of analytical instrumentation.

Skills

Analytical skills

Attention to detail

Communication skills

Independent working

Education

Bachelor's degree in Chemistry or Biochemistry

Tools

Analytical instrumentation

Job description

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan is seeking a qualified Quality Control Chemist I to join our QC team. The role focuses on analytical testing and supporting manufacturing through raw material testing, cleaning verifications, and data documentation.

The candidate should have a Bachelor's degree in Chemistry or Biochemistry and ideally one year of pharmaceutical QC experience, with familiarity in analytical testing and