Senior Pharmaceutical Quality Control Analyst

Placements24

Gauteng

On-site

ZAR 600,000 - 900,000

Full time

3 days ago
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Benefits offered by this job

Medical aid
Retirement fund

Job summary

Placements24 in Midrand, Gauteng, is seeking a Senior Pharmaceutical Quality Control Analyst to lead analytical testing of raw materials, in-process samples, and finished products in a modern QA laboratory.

The role requires a Bachelor’s or Master’s degree in Pharmacy or Chemistry, at least 5 years in a pharma QC lab, and proven expertise in HPLC and GC, GLP/GMP compliance, and data reporting. A competitive annual package includes medical aid and retirement fund contributions.

Qualifications

  • Bachelor’s or Master’s degree in Pharmacy or Chemistry.
  • Minimum 5 years of experience in a pharmaceutical quality control laboratory.
  • Proven expertise with HPLC and GC and GLP/GMP compliance.
  • Strong data analysis and scientific report writing skills.

Responsibilities

  • Perform analytical tests on pharmaceutical products using HPLC, GC, UV-Vis, and titration.
  • Develop and validate analytical methods in line with GLP/GMP.
  • Investigate out-of-specification results and implement CAPAs.
  • Maintain and document laboratory records and test reports.

Skills

HPLC
GC
GLP
GMP
QA experience

Education

Bachelor’s or Master’s degree in Pharmacy or Chemistry

Tools

HPLC systems

Job description

Showing 1303 Senior Pharmaceutical Quality Control Analyst jobs in Midrand

Senior Pharmaceutical Quality Control Analyst

Posted today

Job Description

full-time

About the Role

Our client is seeking a highly motivated and experienced Senior Pharmaceutical Quality Control Analyst to join their dynamic team in Midrand . This critical role will involve conducting rigorous testing and analysis of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with stringent quality standards and regulatory requirements. You will be instrumental in maintaining the integrity and safety of our client's pharmaceutical offerings, working within a state-of-the-art laboratory environment that fosters innovation and scientific excellence. The ideal candidate will possess a strong understanding of analytical techniques and a commitment to upholding the highest levels of quality assurance in the pharmaceutical industry.

Key Responsibilities
  • Perform a wide range of analytical tests on pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
  • Develop and validate new analytical methods as required, ensuring adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Investigate out-of-specification (OOS) results, identify root causes, and implement corrective and preventative actions (CAPAs).
  • Maintain detailed and accurate laboratory records, prepare comprehensive test reports, and manage sample traceability.
  • Calibrate, maintain, and troubleshoot laboratory equipment to ensure accurate and reliable results.
  • Collaborate with R&D, production, and regulatory affairs teams to address quality-related issues and support product development lifecycles.
Requirements
  • Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
  • Minimum of 5 years of experience in a pharmaceutical quality control laboratory setting.
  • Proven expertise in various analytical instrumentation and methodologies, particularly HPLC and GC .
  • Thorough understanding of South African pharmaceutical regulations , GMP, and GLP guidelines.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Proficiency in data analysis and scientific report writing.
Benefits
  • Competitive annual salary with performance-based bonuses.
  • Comprehensive medical aid and retirement fund contributions.
  • Opportunities for professional development, training, and attending industry conferences.
  • Access to cutting-edge laboratory technology and resources.
  • A collaborative and supportive work environment dedicated to quality and compliance in Midrand .
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