Senior Pharmaceutical Quality Control Analyst

Placements24

Soweto

On-site

ZAR 540,000 - 760,000

Full time

3 days ago
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Benefits offered by this job

Competitive salary
Medical coverage
Retirement plan
Performance bonuses
Professional development
Collaborative environment

Job summary

Placements24 is seeking a Senior Pharmaceutical Quality Control Analyst to join our client’s laboratory in Soweto, Gauteng. The role focuses on analytical testing of raw materials, in-process samples, and finished products to ensure GMP compliance and regulatory standards.

You will utilize HPLC, GC, and other techniques, calibrate lab equipment, and contribute to method validation and audits. A Bachelor’s in a related field with 4+ years of QC experience is preferred.

Qualifications

  • Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.
  • Minimum of 4 years' experience in pharmaceutical quality control with hands-on analytical testing.
  • Proficiency with analytical instruments, especially HPLC and GC.
  • Solid understanding of GMP, USP/BP guidelines, and regulatory requirements.
  • Excellent analytical, detail-oriented, and problem-solving skills.
  • Strong written and verbal communication for documentation.
  • Ability to work independently and in a team.
  • Experience with LIMS is a plus.
  • Willingness to work on-site full-time in Soweto.

Responsibilities

  • Perform analytical tests on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, FTIR, and wet chemistry.
  • Analyze results against specifications and document findings accurately.
  • Investigate OOS results and identify root causes, recommending corrective actions.
  • Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance and accuracy.
  • Prepare analytical methods and validation protocols, and execute method validation studies.
  • Maintain laboratory notebooks and records in compliance with GMP and regulatory requirements.
  • Prepare certificates of analysis (CoAs) for released products.
  • Participate in internal and external audits as required.
  • Ensure compliance with all safety procedures and laboratory best practices.
  • Contribute to continuous improvement initiatives within the Quality Control laboratory.

Skills

Analytical testing
GMP knowledge
Detail-oriented
Team collaboration
Problem solving

Education

Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field

Tools

HPLC
GC
UV-Vis spectroscopy
FTIR
Wet chemistry
LIMS

Job description

About the Role

Our client, a reputable pharmaceutical manufacturer, is seeking a diligent and experienced Senior Pharmaceutical Quality Control Analyst to join their laboratory team in Soweto, Gauteng . This critical role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality and regulatory specifications. The ideal candidate will possess a strong foundation in analytical chemistry, hands‑on experience with various laboratory instruments, and a thorough understanding of GMP principles. This is an on‑site position, requiring full‑time commitment within our state‑of‑the‑art laboratory facilities in Soweto . Your meticulous work will be vital in safeguarding the quality and safety of our pharmaceutical products.

Key Responsibilities
  • Perform various analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and wet chemistry.
  • Analyze test results, compare them against established specifications, and document findings accurately.
  • Investigate out-of-specification (OOS) results and identify root causes, recommending corrective actions.
  • Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance and accuracy.
  • Prepare analytical methods and validation protocols, and execute method validation studies.
  • Maintain laboratory notebooks and records in compliance with GMP and regulatory requirements.
  • Prepare certificates of analysis (CoAs) for released products.
  • Participate in internal and external audits as required.
  • Ensure compliance with all safety procedures and laboratory best practices.
  • Contribute to continuous improvement initiatives within the Quality Control laboratory.
Requirements
  • Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Minimum of 4 years of experience in pharmaceutical quality control, with significant hands‑on experience in analytical testing.
  • Proficiency in using and maintaining analytical instruments, particularly HPLC and GC.
  • Solid understanding of GMP principles, pharmaceutical testing guidelines (e.g., USP, BP), and regulatory requirements.
  • Excellent analytical and problem‑solving skills, with a high degree of accuracy and attention to detail.
  • Strong written and verbal communication skills for documentation and reporting.
  • Ability to work effectively both independently and as part of a team.
  • Experience with laboratory information management systems (LIMS) is a plus.
  • Must be able to work full‑time on‑site in Soweto, Gauteng .
  • Demonstrated commitment to quality and safety in a laboratory setting.
Benefits
  • competitive salary
  • comprehensive medical coverage
  • retirement savings plan
  • performance‑based bonuses
  • opportunities for professional development
  • We provide a supportive and collaborative laboratory environment.

Join our dedicated team in Soweto, Gauteng and contribute to ensuring the highest standards of pharmaceutical quality.

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