Pharmaceutical Quality Control Analyst

Placements24; LegKraal Gate; On-site; ZAR 320,000 - 460,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund

Bonus opportunities

Paid leave

Training opportunities

Job summary

Placements24 in Mahikeng, South Africa, is seeking a meticulous Pharmaceutical Quality Control Analyst to ensure the quality and safety of pharmaceutical products. You will perform analytical tests on raw materials, in-process samples, and finished goods in a GMP-compliant lab.

The role requires a Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or related field, plus at least two years' QC experience with HPLC, GC, and dissolution testing.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or related scientific discipline.
• Minimum of 2 years of experience as a QC Analyst in the pharmaceutical industry.
• Hands-on experience with analytical instrumentation such as HPLC, GC, and dissolution testing.
• Solid understanding of GMP, pharmacopeial standards (e.g., USP, BP), and laboratory safety practices.
• Strong attention to detail, accuracy, and record‑keeping skills.
• Ability to work effectively both independently and as part of a team.

Responsibilities

• Perform chemical and physical testing of raw materials, intermediates, and finished pharmaceutical products using various analytical techniques.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Accurately document all testing procedures, results, and observations in laboratory notebooks and electronic systems.
• Conduct method validation and transfer activities as required.
• Investigate out-of-specification (OOS) results and participate in root cause analysis.
• Ensure compliance with GMP, SOPs, and safety regulations within the QC laboratory.

Skills

Attention to detail

Record-keeping

Teamwork

Independent work

Education

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

Tools

HPLC

GC

Dissolution testing

Job description

About the Role

Our client, a prominent pharmaceutical manufacturer in Mahikeng , is looking for a meticulous and technically skilled Pharmaceutical Quality Control Analyst . This role is crucial for ensuring the quality and safety of our client's pharmaceutical products by performing a range of analytical tests on raw materials, in-process samples, and finished goods. You will work within a well-equipped laboratory, adhering strictly to Good Manufacturing Practices (GMP) and standard operating procedures (SOPs). This position is ideal for a budding scientist who is passionate about quality and precision in pharmaceutical production.

Key Responsibilities

• Perform chemical and physical testing of raw materials, intermediates, and finished pharmaceutical products using various analytical techniques.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Accurately document all testing procedures, results, and observations in laboratory notebooks and electronic systems.
• Conduct method validation and transfer activities as required.
• Investigate out-of-specification (OOS) results and participate in root cause analysis.
• Ensure compliance with GMP, SOPs, and safety regulations within the QC laboratory.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or a related scientific discipline.
• Minimum of 2 years of experience as a QC Analyst in the pharmaceutical industry.
• Hands-on experience with analytical instrumentation such as HPLC, GC , and dissolution testing.
• Solid understanding of GMP, pharmacopeial standards (e.g., USP, BP), and laboratory safety practices.
• Strong attention to detail, accuracy, and record‑keeping skills.
• Ability to work effectively both independently and as part of a team.

Benefits

• Competitive salary based on qualifications and experience.
• Comprehensive medical aid and retirement fund contributions.
• Annual performance bonus opportunities.
• Paid leave and company holidays.
• Opportunities for professional development and on-the-job training within a quality-focused environment.