Analytical Scientist: HPLC/GC Method Development

PPL Pharma Solutions Riverview LLC; Riverview (MI); On-site; USD 70,000 - 110,000; Full time

Job summary

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan seeks an Analytical Scientist to join the Analytical Chemistry team. The role focuses on developing and validating analytical methods, primarily HPLC and GC, and ensuring compliant documentation and testing across raw materials, intermediates, and finished products.

The candidate will contribute to method validation, instrument maintenance, and documentation in a fast-paced GMP

Qualifications

• Ph.D. in Chemistry/Biochemistry with 0–3 years’ experience or Masters with 3–5 years or Bachelor’s with 5–10 years in a related environment.
• Experience in analytical method development and validation is required.
• Familiarity with HPLC and GC techniques and associated instrumentation.

Responsibilities

• Develop analytical methods for QC and process development using HPLC/GC.
• Document method development in notebooks for future reference.
• Prepare test methods and supporting documentation for Riverview laboratory use.
• Validate methods for raw materials, intermediates, and finished products; create validation reports.
• Maintain and calibrate analytical instruments such as HPLC and GC; record keeping of maintenance activities.
• Support manufacturing with testing of materials and products; ensure timely test results.
• Maintain QC laboratory inventory and documentation, including retention samples.

Skills

Analytical testing

Instrumentation

Documentation

Attention to detail

Independent work

MS Office / ChemStation

Education

PhD in Chemistry or Biochemistry

MS in Chemistry or Biochemistry

BS in Chemistry or related field

Tools

Agilent ChemStation

Job description

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan seeks an Analytical Scientist to join the Analytical Chemistry team. The role focuses on developing and validating analytical methods, primarily HPLC and GC, and ensuring compliant documentation and testing across raw materials, intermediates, and finished products.

The candidate will contribute to method validation, instrument maintenance, and documentation in a fast-paced GMP