Pharmaceutical Quality Control Chemist

Placements24; Gqeberha; On-site; ZAR 420,000 - 640,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

Paid annual leave

Training & development

Job summary

Placements24 is seeking a Pharmaceutical Quality Control Chemist for a role in Port Elizabeth, Eastern Cape. You will perform analytical testing on raw materials, in-process samples, and finished products to ensure GMP compliance and product safety.

The ideal candidate has a Bachelor's degree in Chemistry or related field, 2–3 years in QC labs, hands-on experience with HPLC/GC, and strong documentation skills. Join a well-established manufacturing facility focused on excellence.

Qualifications

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy or related science.
• 2–3 years of relevant pharmaceutical QC laboratory experience.
• Experience with HPLC/GC and analytical instrumentation is essential.
• GMP knowledge and good documentation practices are required.
• Familiarity with LIMS is a plus.

Responsibilities

• Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished products.
• Operate and maintain HPLC, GC, UV-Vis, FTIR, and dissolution testers.
• Prepare reagents, standards, and samples per approved methods and SOPs.
• Record and document results, deviations, and observations in notebooks and LIMS.
• Review data and assist with method validation and transfer activities.
• Ensure GMP/GLP compliance and maintain laboratory safety.
• Assist CAPA and deviation investigations when needed.
• Maintain cleanliness and organization of the QC lab.

Skills

Analytical chemistry

GMP knowledge

Laboratory documentation

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry/Analytical Chemistry/Pharmacy or related field

Tools

HPLC

GC

UV-Vis spectrophotometers

FTIR

Dissolution testers

Job description

About the Role

Our client, a prominent player in the pharmaceutical manufacturing sector, is seeking a meticulous and dedicated Pharmaceutical Quality Control Chemist to join their team in Port Elizabeth, Eastern Cape . This essential role ensures that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements before release to the market. The ideal candidate will possess strong analytical chemistry skills and a thorough understanding of Good Manufacturing Practices (GMP). You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products. This position is crucial for maintaining the integrity and safety of our client's pharmaceutical offerings. Join a company committed to excellence in quality and patient safety within a well-established manufacturing facility.

Key Responsibilities

• Perform routine and non-routine analytical testing on raw materials, intermediates, and finished pharmaceutical products using various analytical techniques.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, FTIR, and dissolution testers.
• Prepare reagents, standards, and samples for analysis according to approved methods and SOPs.
• Accurately record and document all test results, observations, and deviations in laboratory notebooks and LIMS.
• Review and verify analytical data generated by other QC chemists.
• Participate in method validation and transfer activities.
• Ensure compliance with all GMP, GLP, and safety regulations within the QC laboratory.
• Troubleshoot analytical methods and equipment issues.
• Contribute to deviation investigations and CAPA (Corrective and Preventive Actions) implementation.
• Maintain laboratory cleanliness and organization.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related science field.
• Minimum of 2-3 years of relevant experience in a pharmaceutical Quality Control laboratory.
• Proficiency in operating and maintaining common analytical instruments, particularly HPLC and GC.
• Strong understanding of analytical chemistry principles and techniques.
• Knowledge of GMP and pharmaceutical quality systems is essential.
• Experience with laboratory information management systems (LIMS) is a plus.
• Excellent attention to detail, accuracy, and record-keeping skills.
• Good organizational and time management abilities.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a team in a fast-paced environment.

Benefits

Our client offers a competitive salary package, reflective of your skills and experience, along with comprehensive health and wellness benefits. This includes medical aid, retirement fund contributions, and paid annual leave. Opportunities for on-the-job training and professional development within a stable manufacturing environment are available. You will be working with a dedicated team in Port Elizabeth, Eastern Cape , contributing to the production of high-quality pharmaceutical products. Our client is committed to employee growth and maintaining a safe and supportive workplace.