Pharma QC Analyst: GMP, HPLC, Career Growth

Placements24

United States

Remote

USD 65,000 - 90,000

Full time

2 days ago
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Benefits offered by this job

Competitive salary package
Health, dental, and vision insurance
Retirement savings plan
Paid vacation and sick leave
Career advancement opportunities

Job summary

Placements24 is seeking a meticulous Pharmaceutical Quality Control Analyst to join our established team in George. You will perform analytical tests on raw materials, in-process samples, and finished products to verify regulatory compliance, ensuring safety and quality before reaching patients.

You will calibrate equipment, document data per GLP and GMP, and participate in method validation and transfer activities.

Qualifications

  • Bachelor’s degree in Chemistry, Pharmacy or related field.
  • Experience as a Quality Control Analyst in the pharma industry.
  • Proficiency with HPLC, UV-Vis spectrophotometry and titration.
  • Strong GMP knowledge and regulatory awareness.
  • Attention to detail and accurate data recording.
  • Ability to work independently and in a team in a regulated environment.

Responsibilities

  • Perform routine and non-routine analytical testing of pharmaceutical samples.
  • Calibrate and maintain laboratory equipment.
  • Document testing activities per GLP and regulatory guidelines.
  • Investigate out-of-specification (OOS) results and implement CAPAs.
  • Review and approve analytical data and reports for materials and finished products.
  • Participate in method validation and transfer activities.

Skills

HPLC
UV-Vis spectrophotometry
Titration
GMP
Data integrity
Analytical testing

Education

Bachelor's degree in Chemistry, Pharmacy, or related field

Job description

Placements24 is seeking a meticulous Pharmaceutical Quality Control Analyst to join our established team in George. You will perform analytical tests on raw materials, in-process samples, and finished products to verify regulatory compliance, ensuring safety and quality before reaching patients.

You will calibrate equipment, document data per GLP and GMP, and participate in method validation and transfer activities.

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