QC Analyst – GMP Pharmaceutical Lab & Analytical Chemistry

Assure Infusions; Bartow (FL); On-site; USD 80,000 - 105,000; Full time

Job summary

Assure Infusions in Bartow, FL, seeks a QC Analyst to perform routine and non-routine analytical testing in a GMP-regulated pharmaceutical manufacturing environment. The role requires a strong background in small molecule analytics, compendial methods, and laboratory quality systems.

You will support investigations, CAPAs, and deviations, with responsibility for data integrity, documentation, and cross-functional collaboration with QA, Manufacturing, and Validation teams.

Qualifications

• Bachelor’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biology, Biochemistry, or related field.
• Minimum 5 years of experience in GMP pharmaceutical QC or related regulated laboratory.
• Strong background in small molecule QC analytics, compendial testing, and data integrity.

Responsibilities

• Perform routine and non-routine QC analytical testing per approved procedures and GMP.
• Coordinate raw material sampling, testing, and release activities.
• Investigate deviations, CAPAs, and OOS events with proper documentation.
• Review data for accuracy and ensure compliance with ALCOA+ and GMP.

Skills

GMP QC

Technical writing

Data integrity

Independent worker

Education

Bachelors in Chemistry

Tools

Empower

LIMS

Electronic QA systems

Job description

Assure Infusions in Bartow, FL, seeks a QC Analyst to perform routine and non-routine analytical testing in a GMP-regulated pharmaceutical manufacturing environment. The role requires a strong background in small molecule analytics, compendial methods, and laboratory quality systems.

You will support investigations, CAPAs, and deviations, with responsibility for data integrity, documentation, and cross-functional collaboration with QA, Manufacturing, and Validation teams.