Quality Control Analyst - Pharmaceutical

Placements24; Rustenburg; On-site; ZAR 450,000 - 600,000; Full time

Benefits offered by this job

Competitive salary

Health, disability & life insurance

Pension fund contribution

Paid time off and company holidays

Training & growth

Job summary

Placements24 is seeking a meticulous Quality Control Analyst for our Rustenburg facility to ensure pharmaceutical products meet quality, safety, and efficacy standards. You will conduct tests on raw materials, in-process samples, and finished products using HPLC, GC, and spectrophotometric methods.

The role requires a Bachelor's in Chemistry or Pharmaceutical Sciences, 2+ years in QC labs, strong documentation, and GMP/GLP knowledge; on-site position with a competitive salary and benefits.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.
• 2+ years in a pharmaceutical QC laboratory setting.
• Proficiency with analytical techniques and instrumentation (HPLC, GC, UV-Vis).
• GMP/GLP knowledge and strong documentation skills.

Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished products.
• Operate and maintain laboratory instruments such as HPLC, GC, spectrophotometers, and dissolution apparatus.
• Analyze test results, document findings, and report deviations or out-of-spec results promptly.
• Participate in method development and validation activities for new procedures.
• Ensure GMP/GLP compliance in laboratory operations in Rustenburg.

Skills

Analytical testing

Laboratory instrumentation

HPLC

GC

UV-Vis

Documentation

Education

Bachelor's degree in Chemistry/Pharmaceutical Sciences

Tools

HPLC

GC

UV-Vis spectrophotometer

Dissolution apparatus

Job description

About the Role

Our client is looking for a meticulous and experienced Quality Control Analyst to join their state-of-the-art facility in Rustenburg . This role is critical in ensuring that all pharmaceutical products manufactured meet the highest standards of quality, safety, and efficacy. You will perform a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment. Your work will directly contribute to the company's commitment to regulatory compliance and customer satisfaction, maintaining the integrity of our client's reputation in the pharmaceutical industry.

Key Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished pharmaceutical products according to established specifications and SOPs.
• Operate and maintain various laboratory instruments such as HPLC, GC, spectrophotometers, and dissolution apparatus.
• Analyze test results, document findings accurately, and report any deviations or out-of-specification results promptly.
• Participate in method development and validation activities for new analytical procedures.
• Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in all laboratory operations within Rustenburg .

Requirements

• A Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Proven experience (2+ years) in a pharmaceutical quality control laboratory setting.
• Proficiency with analytical techniques and instrumentation commonly used in the pharmaceutical industry (e.g., HPLC, GC, UV-Vis).
• Strong understanding of GMP/GLP regulations and quality control principles.
• Excellent documentation skills and attention to detail for accurate record-keeping.

Benefits

• Competitive annual salary commensurate with experience.
• Comprehensive health, disability, and life insurance coverage.
• Pension fund contribution.
• Paid time off and company holidays.
• Opportunities for further training and professional growth within the quality assurance field in Rustenburg .