Pharmaceutical Quality Control Analyst

Placements24; United States; Remote; USD 65,000 - 90,000; Full time

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

About the Role

Our client is seeking a meticulous Pharmaceutical Quality Control Analyst to join their established team in George . This role is essential for ensuring the safety, efficacy, and quality of pharmaceutical products manufactured by the company. You will perform a wide range of analytical tests on raw materials, in-process samples, and finished products to verify compliance with stringent regulatory standards. The successful candidate will work in a well-equipped laboratory, contributing to the overall quality assurance framework and supporting the company's commitment to excellence in pharmaceutical manufacturing, ensuring that every product meets the highest standards before it reaches the patient.

Key Responsibilities

• Perform routine and non-routine analytical testing of pharmaceutical samples using various laboratory techniques.
• Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
• Document all testing activities meticulously in accordance with Good Laboratory Practices (GLP) and regulatory guidelines.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
• Review and approve analytical data and reports for raw materials and finished products.
• Participate in method validation and transfer activities as required.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related scientific discipline.
• Proven experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency in analytical techniques such as HPLC , UV-Vis spectrophotometry, and titration.
• Thorough understanding of GMP (Good Manufacturing Practices) and regulatory requirements.
• Strong attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a regulated environment.

Benefits

• Competitive salary package.
• Health, dental, and vision insurance plans.
• Retirement savings plan.
• Paid vacation and sick leave.
• Opportunities for career advancement within a reputable pharmaceutical company.