QC Analyst I — GMP Lab Testing & Documentation

JobRx, Inc.; Sellersville (Bucks County); On-site; USD 52,000 - 70,000; Full time

Job summary

Piramal Pharma Solutions is seeking a QC Analyst I to join our Quality Control team in Sellersville, PA. This role performs analytical and physical testing of raw materials, finished products, and stability samples in accordance with approved procedures and cGMP.

The candidate will support laboratory operations through accurate testing, reagent preparation, data entry, and GDP-compliant documentation, ensuring regulatory and quality standards are met.

Qualifications

• Bachelor's degree in Chemistry, Biology, Microbiology, or another related scientific discipline with relevant laboratory coursework.
• 1-2 years of laboratory experience, preferably within a GMP-regulated environment.
• Experience in pharmaceutical, biotechnology, or other regulated laboratory environments.
• Experience utilizing Laboratory Information Management Systems (LIMS).
• Familiarity with compendial testing requirements and pharmaceutical quality systems.

Responsibilities

• Perform analytical and physical testing of raw materials, finished products, and stability samples.
• Accurately document laboratory activities and test results per GDP.
• Prepare reagents and lab materials for testing activities.
• Follow cGMP and FDA regulatory requirements; support investigations and audits.
• Maintain clean and organized laboratory workspace; participate in continuous improvement.

Skills

Attention to detail

Organizational skills

Communication skills

Multitasking

Education

Bachelor's degree in Chemistry or related sciences

Tools

LIMS

FTIR

Dissolution testing

UV-Vis spectroscopy

Job description

Piramal Pharma Solutions is seeking a QC Analyst I to join our Quality Control team in Sellersville, PA. This role performs analytical and physical testing of raw materials, finished products, and stability samples in accordance with approved procedures and cGMP.

The candidate will support laboratory operations through accurate testing, reagent preparation, data entry, and GDP-compliant documentation, ensuring regulatory and quality standards are met.