Quality Control Analyst

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

About the Role

Our client is seeking a meticulous and detail-oriented Quality Control Analyst to join their esteemed pharmaceutical team based in Tembisa. This role is integral to ensuring the consistent quality and safety of pharmaceutical products by performing rigorous testing and analysis. You will operate within a highly regulated environment, upholding the highest standards of quality assurance. This position offers the chance to contribute directly to product integrity and patient safety, working with a dedicated team focused on excellence in pharmaceutical manufacturing and quality control.

Key Responsibilities

• Perform routine quality control testing on raw materials, in-process samples, and finished products using various analytical techniques.
• Accurately document all testing procedures, results, and observations in accordance with GxP guidelines.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and compliance with calibration schedules.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Prepare Certificates of Analysis (CoA) and other quality-related documentation.
• Stay updated on relevant regulatory requirements and internal quality standards.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Proven experience (2+ years) in a pharmaceutical quality control or quality assurance role.
• Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and dissolution apparatus.
• Strong understanding of GxP (Good Manufacturing Practices, Good Laboratory Practices) principles.
• Excellent documentation skills and attention to detail are essential.
• Ability to work independently and collaboratively within a team environment.

Benefits

• Competitive annual salary commensurate with experience.
• Comprehensive medical aid and retirement fund contributions.
• Paid annual leave and other statutory benefits.
• Opportunities for training in advanced analytical techniques and quality systems.
• A secure and professional working environment committed to employee growth.