Pharmaceutical Quality Control Analyst

Placements24; Kempton Park; On-site; ZAR 350,000 - 520,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Provident fund

Professional development

Modern processes

Stable environment

Annual bonus

Job summary

Placements24 is seeking a Pharmaceutical Quality Control Analyst for their on-site facility in Gauteng. The role focuses on ensuring the quality and safety of pharmaceutical products through analytical testing and strict adherence to GMP and GLP standards.

You will work with HPLC, GC and other instruments, document results, report deviations, and collaborate with R&D, Production and QA to resolve issues. A relevant degree and 3+ years' lab experience are required, with SAHPRA compliance

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related field.
• Minimum of 3 years in a pharmaceutical quality control laboratory.
• Proficiency with HPLC, GC, dissolution testers and spectrophotometers.
• Strong GMP knowledge and familiarity with regulatory guidelines.
• Excellent analytical skills with meticulous attention to detail.
• Proficiency in data analysis and report writing.
• Ability to work independently and in a team in a fast-paced environment.
• Good written and verbal communication skills.
• Based in or willing to relocate to the Tembisa, Gauteng area.

Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis, and FTIR.
• Validate and calibrate laboratory equipment to ensure accurate results.
• Document testing procedures, results, and deviations per GLP and SOPs.
• Analyze test data, prepare Certificates of Analysis (CoA), and report any out-of-spec results.
• Participate in method development and validation studies for new analytical methods.
• Maintain laboratory inventory, including reagents and consumables, and ensure a safe working environment.
• Collaborate with R&D, Production, and Quality Assurance to resolve quality issues.
• Adhere to safety protocols and regulatory requirements, including SAHPRA.

Skills

Analytical testing

Data analysis

Report writing

Teamwork

Communication skills

Independent worker

Education

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

Tools

HPLC

GC

Dissolution testers

Spectrophotometers

Job description

About the Role Our client, a rapidly growing pharmaceutical manufacturing company, is looking for a dedicated Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in Tembisa, Gauteng. This role is crucial for ensuring the consistent quality and safety of pharmaceutical products before they reach the market. The successful candidate will be responsible for performing a variety of analytical tests and ensuring compliance with stringent industry standards. This is an on-site position offering a stable career path within a company committed to producing high-quality medicines. If you have a keen eye for detail and a passion for pharmaceutical quality, this is an excellent opportunity to contribute significantly to public health and safety in South Africa.

Key Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Validate and calibrate laboratory equipment to ensure accuracy and reliability of results.
• Document all testing procedures, results, and deviations in accordance with Good Laboratory Practices (GLP) and company SOPs.
• Analyze test data, prepare Certificates of Analysis (CoA), and report any out-of-specification (OOS) results.
• Participate in method development and validation studies for new analytical methods.
• Maintain laboratory inventory, including reagents and consumables, and ensure a safe working environment.
• Collaborate with R&D, Production, and Quality Assurance departments to resolve quality issues.
• Adhere to all safety protocols and regulatory requirements, including those set by SAHPRA.

Requirements

• A Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
• Minimum of 3 years of hands-on experience in a pharmaceutical quality control laboratory.
• Proficiency with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Strong understanding of pharmaceutical quality systems, GMP, and regulatory guidelines.
• Excellent analytical skills with meticulous attention to detail.
• Proficiency in data analysis and report writing.
• Ability to work independently and as part of a team in a fast-paced environment.
• Good communication skills, both written and verbal.
• Must be based in or willing to relocate to the Tembisa, Gauteng area.

Benefits

• Competitive salary package.
• Medical aid and provident fund.
• Opportunities for further training and professional development in quality assurance.
• Exposure to modern pharmaceutical manufacturing processes.
• A stable and secure work environment within a growing company.
• Annual performance bonus.