Pharma QC Analyst - Precision Testing & Compliance

Placements24; Gauteng; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund contributions

Paid annual leave

Training in analytical techniques

Growth-oriented environment

Job summary

Placements24 in Gauteng seeks a meticulous Quality Control Analyst for a pharmaceutical team in Tembisa. You will perform routine QC testing on materials and products, document results, calibrate equipment, and investigate deviations to uphold product safety and quality.

The role requires a relevant scientific degree and 2+ years in QC/QA, with strong GxP knowledge and precise documentation. A supportive, compliant lab environment awaits.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmacy or related scientific discipline.
• Experience (2+ years) in pharmaceutical quality control/assurance.
• Proficiency with analytical instrumentation and GxP compliance.
• Strong documentation and attention to detail.

Responsibilities

• Perform routine quality control testing on raw materials, in-process samples and finished products.
• Document testing procedures, results and observations in line with GxP.
• Calibrate and maintain laboratory equipment and calibration schedules.
• Investigate OOS results and deviations, participate in root cause analysis.
• Prepare Certificates of Analysis and related quality documentation.
• Stay updated on regulatory requirements and internal standards.

Skills

HPLC

GC

UV-Vis spectrophotometry

Dissolution apparatus

GxP principles

Documentation

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry, Biochemistry, Pharmacy

Job description

Placements24 in Gauteng seeks a meticulous Quality Control Analyst for a pharmaceutical team in Tembisa. You will perform routine QC testing on materials and products, document results, calibrate equipment, and investigate deviations to uphold product safety and quality.

The role requires a relevant scientific degree and 2+ years in QC/QA, with strong GxP knowledge and precise documentation. A supportive, compliant lab environment awaits.