Pharmaceutical Quality Control Analyst

Placements24

Paarl

On-site

ZAR 420,000 - 540,000

Full time

2 days ago
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Benefits offered by this job

Medical and dental insurance
Retirement savings plan
Professional development opportunities
Modern laboratory facilities

Job summary

Placements24 is seeking a Pharmaceutical Quality Control Analyst for an on-site role in Paarl, Western Cape. The candidate will perform analytical tests on materials and finished products, using HPLC/GC, UV-Vis, and dissolution equipment, with strict data recording and compliance to GMP/GLP.

The role requires a science degree and 2–3 years in a QC lab, strong attention to detail, and ability to work both independently and in a team within a dynamic pharmaceutical environment.

Qualifications

  • Bachelor’s degree in Chemistry or Pharmacy or related field.
  • Minimum 2–3 years in a pharmaceutical QC laboratory setting.
  • Hands-on with HPLC and GC and familiarity with pharmacopoeial methods (USP/BP/EP).
  • Proficient in data recording, analysis, and GMP/GLP compliance.
  • Excellent attention to detail and documentation discipline.

Responsibilities

  • Perform analytical tests on raw materials, intermediates, and finished products per SOPs.
  • Operate and maintain HPLC, GC, UV-Vis, dissolution testers, and titrators.
  • Prepare reagents and solutions for analyses and record results accurately.
  • Review data and deviations, participate in investigations for out-of-spec results.
  • Assist in method development and validation; ensure GLP and GMP adherence.
  • Maintain a clean, safe lab and participate in audits as needed.

Skills

Analytical testing
Data analysis
Attention to detail
Time management
Teamwork

Education

Bachelor's degree in Chemistry or Pharmacy

Tools

HPLC
GC
UV-Vis spectrophotometers
Dissolution testers
Titrators

Job description

About the Role

Our client, a leading pharmaceutical manufacturer dedicated to producing safe and effective medications, is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their laboratory team in Paarl, Western Cape . This role is essential for ensuring that all raw materials, in-process samples, and finished products meet stringent quality specifications and regulatory standards. The successful candidate will perform a variety of analytical tests using advanced laboratory equipment and will be responsible for accurate data recording and reporting. This is a hands‑on laboratory position that requires a strong foundation in analytical chemistry and a commitment to quality. The role is based on‑site in the scenic Winelands region of Paarl, Western Cape .

Key Responsibilities
  • Perform a wide range of analytical tests on raw materials, intermediates, and finished pharmaceutical products according to approved methods and specifications.
  • Operate and maintain laboratory equipment such as HPLC, GC, UV‑Vis spectrophotometers, dissolution testers, and titrators.
  • Prepare reagents and solutions required for analytical testing.
  • Accurately document all experimental procedures, results, and observations in laboratory notebooks and electronic systems.
  • Review and verify data generated by other analysts, ensuring compliance with quality standards.
  • Identify and report any out‑of‑specification (OOS) results or deviations, participating in investigations as required.
  • Assist in the development and validation of new analytical methods.
  • Ensure laboratory adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Maintain a clean, organized, and safe laboratory environment.
  • Participate in internal and external audits as needed.
Requirements
  • Bachelor's degree in Chemistry, Pharmacy, or a related scientific discipline.
  • Minimum of 2-3 years of experience in a pharmaceutical quality control laboratory setting.
  • Hands‑on experience with analytical techniques, particularly HPLC and GC.
  • Familiarity with pharmacopoeial methods (e.g., USP, BP, EP).
  • Proficiency in laboratory software and data analysis.
  • Strong understanding of GMP and GLP principles.
  • Excellent attention to detail and accuracy in testing and documentation.
  • Good organizational and time management skills.Ability to work effectively both independently and as part of a team.
  • Strong problem‑solving abilities.
Benefits
  • Our client offers a competitive salary, comprehensive medical and dental insurance, and a retirement savings plan.
  • We provide opportunities for professional development, including training on new analytical techniques and equipment.
  • Employees benefit from a supportive team environment, access to modern laboratory facilities, and the chance to contribute to the production of high‑quality medicines in the beautiful Paarl, Western Cape region.
  • Our client is committed to fostering a culture of scientific excellence and employee well‑being.
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