HPAPI QC Chemist - Analytical & Quality Control

Piramal Pharma Ltd; Riverview (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan, seeks a qualified Quality Control Chemist I to join the QC team. The role provides analytical chemistry support and ensures compliance through accurate testing and documentation.

Responsibilities include testing materials, verifications, data entry, and participation in methods development/validation projects.Bachelor’s in Chemistry/Biochem preferred; one year QC experience desirable.

Qualifications

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

Responsibilities

• Support manufacturing operations by testing raw and starting materials to meet timelines.
• Perform cleaning verifications on multi-use equipment.
• Test reference standards and stability samples.
• Document preparation, equipment setup and results with accuracy.
• Test intermediates and final products as required.
• Assist in revision of documentation and maintenance of QC records.
• Participate in quality projects including method development/validation and training.
• Support calibration and maintenance of laboratory instrumentation.
• Maintain clean, organized bench areas and lab space.
• Conduct routine testing on the water system and prepare reports.

Skills

Analytical skills

Organizational & planning

Written & verbal communication

Attention to detail

Independent work

Education

Bachelor’s degree in Chemistry/Biochemistry

1 year pharma QC experience

Familiarity with analytical testing & instrumentation

Job description

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan, seeks a qualified Quality Control Chemist I to join the QC team. The role provides analytical chemistry support and ensures compliance through accurate testing and documentation.

Responsibilities include testing materials, verifications, data entry, and participation in methods development/validation projects.Bachelor’s in Chemistry/Biochem preferred; one year QC experience desirable.