Quality Control Analyst

Placements24; Pretoria; On-site; ZAR 300,000 - 420,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Retirement fund contributions

Paid annual leave

Job summary

Placements24 is seeking a detail-oriented Quality Control Analyst to join their manufacturing facility in Pretoria. The role ensures pharmaceutical products meet quality standards and regulatory requirements before release, performing analytical tests and interpreting results.

You will operate lab equipment, maintain calibration, and document findings while adhering to GMP and safety procedures. The position offers collaboration across teams to uphold quality in the pharmaceutical supply chain.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• 1-3 years of experience in a pharmaceutical quality control laboratory setting.
• Proficiency with analytical techniques such as HPLC, UV-Vis spectrophotometry, and dissolution testing.

Responsibilities

• Perform routine analytical testing of raw materials, in-process samples, and finished products using validated methods.
• Operate and maintain laboratory equipment, ensuring proper calibration and functioning.
• Accurately record and report test results, investigate any out-of-specification (OOS) results, and assist in root cause analysis.
• Adhere strictly to Good Manufacturing Practices (GMP) and laboratory safety procedures.
• Maintain laboratory documentation and records in compliance with regulatory standards.
• Participate in method validation and transfer activities as required.

Skills

HPLC

UV-Vis spectrophotometry

Dissolution testing

GMP compliance

Education

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

Job description

About the Role

Our client is seeking a detail-oriented Quality Control Analyst to join their manufacturing facility in Pretoria . This role is essential in ensuring that all pharmaceutical products manufactured meet stringent quality standards and regulatory requirements before release to the market. You will perform a variety of analytical tests, interpret results, and contribute to the maintenance of a robust quality system. This position offers the chance to work in a critical role within the pharmaceutical supply chain, contributing to public health and safety.

Key Responsibilities

• Perform routine analytical testing of raw materials, in-process samples, and finished products using validated methods.
• Operate and maintain laboratory equipment, ensuring proper calibration and functioning.
• Accurately record and report test results, investigate any out-of-specification (OOS) results, and assist in root cause analysis.
• Adhere strictly to Good Manufacturing Practices (GMP) and laboratory safety procedures.
• Maintain laboratory documentation and records in compliance with regulatory standards.
• Participate in method validation and transfer activities as required.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• 1-3 years of experience in a pharmaceutical quality control laboratory setting.
• Proficiency with analytical techniques such as HPLC, UV-Vis spectrophotometry, and dissolution testing.
• Familiarity with GMP guidelines and pharmacopeial standards (e.g., USP, EP).
• Strong attention to detail and ability to follow standard operating procedures meticulously.
• Effective communication and teamwork skills, necessary for collaboration in the Pretoria facility.

Benefits

• Competitive annual salary and potential for performance-based increases.
• Comprehensive health insurance coverage.
• Retirement fund contributions.
• Paid annual leave and sick leave.
• A stable and professional working environment focused on quality and compliance.