Quality Control Analyst - Pharmaceutical

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

Benefits offered by this job

Health insurance

Retirement savings plan

Training and career development

On-site role

Job summary

Placements24 is seeking a meticulous Quality Control Analyst for a pharmaceutical QC role in Polokwane, Limpopo. You will perform analytical testing across raw materials, in-process samples, and finished products, ensuring GMP compliance and data integrity in a modern lab.

The ideal candidate has a Chemistry-related degree and at least 2 years’ QC experience, with hands-on use of HPLC, GC, Karl Fischer, and dissolution testing. Knowledge of pharmacopoeial standards is essential.

Qualifications

• Bachelor's degree in Chemistry or related field.
• Minimum 2 years in pharmaceutical QC lab.
• Experience with HPLC, GC, Karl Fischer, dissolution testing.
• Knowledge of GMP, GLP, pharmacopoeial standards (USP/BP/EP).

Responsibilities

• Perform analytical tests on raw materials, intermediates, and finished products.
• Prepare samples and reagents for testing.
• Operate, calibrate, and maintain laboratory equipment.
• Record, analyze, and ensure compliance with specifications.

Skills

HPLC

GC

Karl Fischer

Dissolution

GMP

Pharmacopoeias

Analytical chemistry

Education

Bachelor's degree in Chemistry

Job description

About the Role

Our client, a reputable pharmaceutical manufacturing company, is seeking a meticulous Quality Control Analyst to join their laboratory team in Polokwane, Limpopo. This role is essential for ensuring the quality, safety, and efficacy of pharmaceutical products by performing a variety of analytical tests on raw materials, in-process samples, and finished goods. The ideal candidate possesses a strong foundation in analytical chemistry, experience with relevant laboratory instrumentation, and a keen eye for detail. You will work in a modern laboratory environment, adhering strictly to Good Manufacturing Practices (GMP) and internal quality standards. This is a significant opportunity to contribute to public health by maintaining the highest quality standards for pharmaceutical products in South Africa. We are looking for a dedicated professional committed to scientific accuracy and regulatory compliance.

Key Responsibilities

• Perform a range of analytical tests on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, Titration).
• Prepare samples and reagents for testing.
• Operate, calibrate, and maintain laboratory equipment.
• Record and analyze test results accurately, ensuring compliance with specifications and pharmacopoeial standards.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Maintain detailed and accurate laboratory records and documentation in accordance with GMP.
• Ensure laboratory supplies are managed and that equipment is properly maintained.
• Assist in the validation of analytical methods and equipment qualification.
• Stay updated on current Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Participate in internal and external quality audits as required.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 2 years of experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with analytical techniques such as HPLC, GC, Karl Fischer titration, and dissolution testing.
• Familiarity with pharmacopoeial standards (e.g., USP, BP, EP) and regulatory guidelines.
• Strong understanding of GMP principles and quality systems.
• Excellent analytical, problem-solving, and documentation skills.
• Proficiency in using laboratory software and data analysis tools.
• Ability to work independently and collaboratively in a team environment.
• Good organizational skills and attention to detail.
• Experience with stability testing is a plus.

Benefits

• Our client offers a competitive salary, comprehensive health insurance, retirement savings plan, and opportunities for training and career development.
• This on-site role provides a stable and rewarding career within our Polokwane facility.
• We value our employees and offer generous paid time off, fostering a positive and productive work environment.
• This position is critical to ensuring the quality and safety of medicines manufactured by our client.