QC Analyst II - GMP Lab (LC/GC & HPLC)

Piramal Pharma Limited; Northern (KY); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Piramal Pharma Solutions in Sellersville, PA, seeks a Quality Control Analyst II to perform routine analytical testing using GC, HPLC and UPLC to support product release and stability studies. Strong chromatography skills, method compliance and GDP documentation are required.

The candidate will prepare samples, calibrate instruments, review data in Empower, investigate deviations, and collaborate with QA, Manufacturing and R&D to maintain GMP/GDP standards.

Qualifications

• Bachelor's degree in Chemistry, Biology, Microbiology or related scientific discipline with relevant lab coursework.
• Minimum 2 years of laboratory experience in a GMP-regulated environment.
• Hands-on experience with wet chemistry, chromatographic analysis and instrument operation.

Responsibilities

• Perform qualitative and quantitative analysis using GC, HPLC and UPLC per approved methods and SOPs.
• Prepare samples, standards, diluents and mobile phases following established lab procedures and GDP practices.
• Execute instrument setup, calibration, and system suitability checks; maintain accurate records.
• Process, interpret and review chromatographic data using Empower or equivalent software.
• Investigate atypical results or method deviations and participate in CAPA where needed.
• Support method transfers, verifications, and validations by generating high-quality analytical data.
• Maintain laboratory readiness and ensure safety compliance and proper labeling.

Skills

GC/HPLC/UPLC

Empower software

GDP/GMP knowledge

Documentation practices

Analytical technique knowledge

Education

Bachelor's degree in Chemistry, Biology, or Microbiology

Tools

FTIR

Karl Fischer

Dissolution testing

Job description

Piramal Pharma Solutions in Sellersville, PA, seeks a Quality Control Analyst II to perform routine analytical testing using GC, HPLC and UPLC to support product release and stability studies. Strong chromatography skills, method compliance and GDP documentation are required.

The candidate will prepare samples, calibrate instruments, review data in Empower, investigate deviations, and collaborate with QA, Manufacturing and R&D to maintain GMP/GDP standards.