Quality Control Analyst

Piramal Pharma Solutions; Sellersville (Bucks County); On-site; USD 55,000 - 75,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Chemistry Analyst II to perform routine analytical testing using GC, HPLC and UPLC techniques in a GMP/GLP laboratory. You will prepare samples and standards, operate instruments, process data, and contribute to method transfers and investigations.

The role requires strong chromatographic skills, documentation discipline, and collaboration with QA, Manufacturing, and R&D teams to support product release and stability studies.

Qualifications

• Experience with GC, HPLC and UPLC analytical techniques.
• Strong GMP/GLP laboratory experience and documentation practices.
• Proficiency in data processing and chromatographic data interpretation.

Responsibilities

• Perform qualitative and quantitative analysis using GC, HPLC, UPLC and related systems.
• Prepare samples, standards, diluents, and mobile phases per SOPs and GDP guidelines.
• Execute instrument setup, calibration and system suitability checks; maintain instrument performance.

Skills

GC

HPLC

UPLC

Empower

LIMS

Tools

Empower

LIMS

Job description

The Chemistry Analyst II performs routine analytical testing using Liquid Chromatography (LC) and Gas Chromatography (GC) techniques in support of product release, stability and studies. This role requires strong technical competency in chromatographic analysis, sample preparation, instrument operation, data processing, and troubleshooting within a GMP/GLP laboratory environment.

The Chemistry Analyst II performs routine analytical testing using Liquid Chromatography (LC) and Gas Chromatography (GC) techniques in support of product release, stability and studies. This role requires strong technical competency in chromatographic analysis, sample preparation, instrument operation, data processing, and troubleshooting within a GMP/GLP laboratory environment.

Key Responsibilities

• Perform qualitative and quantitative analysis using GC, HPLC, UPLC, and related chromatographic systems in accordance with approved test methods and SOPs.
• Prepare samples, standards, diluents, and mobile phases following established laboratory procedures and good documentation practices.
• Execute instrument setup, calibration, system suitability checks, and routine maintenance to ensure reliable performance.
• Process, integrate, and interpret chromatographic data using software such as Empower or equivalent.
• Review chromatograms for peak integrity, retention time consistency, baseline quality, and compliance with system suitability criteria.
• Document all analytical activities in laboratory notebooks, LIMS, and controlled forms in accordance with GDP and regulatory expectations.
• Conduct investigations into atypical results, instrument issues, or method deviations, including root‑cause analysis and corrective actions.
• Support method transfers, verifications, and validations by executing protocols and generating high‑quality analytical data.
• Maintain laboratory readiness by ensuring proper reagent labeling, instrument logbook completion, and adherence to safety and compliance requirements.
• Collaborate with cross‑functional teams (QA, Manufacturing, R&D) to support testing priorities and resolve technical issues.