Pharmaceutical Quality Control Analyst

Placements24; Kimberley; On-site; ZAR 300,000 - 500,000; Full time

Benefits offered by this job

Competitive salary

Medical aid contributions

Pension fund participation

Paid annual leave

On-the-job training

Job summary

Placements24 is seeking a meticulous Pharmaceutical Quality Control Analyst to join a Kimberley QC laboratory. The role focuses on analytical testing of raw materials, in-process samples and finished products, using methods and instruments such as HPLC, GC, UV-Vis, FTIR and dissolution testing.

The ideal candidate holds a chemistry-related bachelor's degree and 2–4 years' QC lab experience with GMP knowledge, data documentation, and teamwork skills to ensure quality and regulatory compliance.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Chemistry, Biochemistry or related
• 2–4 years in pharmaceutical QC lab
• Hands-on with HPLC, GC, titration, dissolution and spectroscopy
• Strong GMP understanding and lab procedures
• Proficiency with LIMS desirable

Responsibilities

• Perform analytical testing on raw materials, in-process samples and finished products
• Operate and maintain laboratory equipment (HPLC, GC, UV-Vis, FTIR, dissolution)
• Prepare reagents and solutions for testing
• Document results per GMP and QA requirements
• Review data for accuracy and compliance
• Assist in method validation and verification activities
• Troubleshoot equipment and analytical issues
• Maintain clean, organized lab environment
• Ensure safety and regulatory compliance
• Support investigations of out-of-specification results

Skills

Analytical testing

GMP knowledge

Attention to detail

Teamwork

Problem solving

Education

Bachelor's degree in Chemistry/Pharmaceutical Chemistry/Biochemistry

Tools

HPLC

GC

UV-Vis spectrophotometers

FTIR

Dissolution apparatus

LIMS

Job description

About the Role

Our client, a reputable pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their QC laboratory team in Kimberley, Northern Cape . This role is essential for ensuring the quality and compliance of raw materials, in-process samples, and finished pharmaceutical products through rigorous analytical testing. You will perform a variety of analytical tests using established methods and sophisticated instrumentation. The ideal candidate will have a strong background in analytical chemistry, experience with common QC laboratory techniques, and a thorough understanding of GMP principles. This is an excellent entry-level to mid-level opportunity for a motivated individual passionate about pharmaceutical quality.

Key Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished products according to approved specifications and methods.
• Operate and maintain laboratory equipment, including HPLC, GC, UV-Vis spectrophotometers, FTIR, and dissolution apparatus.
• Prepare reagents and solutions accurately for analytical testing.
• Document all laboratory activities, results, and observations meticulously in accordance with GMP requirements.
• Review and verify analytical data, ensuring accuracy and compliance with specifications.
• Participate in method validation and verification activities as required.
• Troubleshoot equipment malfunctions and analytical issues, escalating as necessary.
• Maintain a clean and organized laboratory environment.
• Ensure compliance with all safety procedures and environmental regulations.
• Assist in the investigation of out-of-specification (OOS) results.

Requirements

• Bachelor's degree in Chemistry, Pharmaceutical Chemistry, Biochemistry, or a related scientific discipline.
• Minimum of 2-4 years of experience working in a pharmaceutical Quality Control laboratory.
• Hands-on experience with analytical techniques such as HPLC, GC, titration, dissolution testing, and spectroscopy.
• Good understanding of Good Manufacturing Practices (GMP) and laboratory procedures.
• Proficiency in using laboratory information management systems (LIMS) is desirable.
• Strong analytical and problem-solving skills.
• Excellent attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team.
• Good written and verbal communication skills.
• Basic understanding of pharmaceutical regulations.

Benefits

• Competitive salary based on experience and qualifications.
• Medical aid contributions.
• Pension fund participation.
• Paid annual leave.
• Opportunities for on-the-job training and skill development.
• Stable and secure working environment.
• Exposure to diverse pharmaceutical products and testing methodologies.
• Contribution to ensuring the safety and efficacy of medicines.