Senior Pharmaceutical Quality Control Analyst

Placements24; East London; Sur place; ZAR 700 000 - 1 000 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Medical aid

Provident fund

Performance-based bonuses

Professional development

Work-life balance

Résumé du poste

Placements24 in East London, Eastern Cape, is seeking a Senior Pharmaceutical Quality Control Analyst to join our laboratory team. You will perform analytical testing on raw materials, intermediates and finished products, ensuring GMP compliance.

The ideal candidate holds a Bachelor's or Master's in Chemistry or Pharmaceutical Sciences with 5–7 years in QC, and is proficient with HPLC, GC, spectrophotometers and dissolution apparatus, plus strong data interpretation and reporting.

Qualifications

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
• 5–7 years of pharmaceutical QC laboratory experience.
• Experience with HPLC, GC, UV-Vis, and dissolution testing.
• Strong GMP/GLP knowledge and method validation experience.
• Excellent data analysis and documentation skills.

Responsabilités

• Perform analytical tests on raw materials, intermediates and finished products using techniques such as HPLC, GC, UV-Vis and Karl Fischer titration.
• Develop, validate, and transfer analytical methods per regulatory guidelines.
• Calibrate, maintain, and troubleshoot laboratory equipment to ensure accurate results.
• Interpret data, document results, and prepare comprehensive reports.
• Investigate OOS and deviations; identify root causes and corrective actions.
• Ensure GMP/GLP and pharmacopoeial compliance and maintain records.
• Participate in audits and assist in training junior QC analysts.
• Stay updated on analytical techniques and QC methodologies.

Connaissances

Data analysis

Interpretation

Problem solving

Communication

Teamwork

Formation

Bachelor's or Master's in Chemistry

Analytical Chemistry

Pharmaceutical Sciences

Outils

HPLC

GC

Spectrophotometers

Dissolution apparatus

LIMS

Description du poste

About the Role

Our client, a dynamic and growing pharmaceutical manufacturing company, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their laboratory team in East London . This role is critical for ensuring the quality and compliance of raw materials, in-process samples, and finished pharmaceutical products through rigorous analytical testing. You will perform a variety of chemical and physical tests using advanced laboratory instrumentation and adhere strictly to Good Manufacturing Practice (GMP) and other relevant regulatory standards. This is an excellent opportunity for a skilled analyst to contribute to product integrity and patient safety within a reputable organization. The position is based in East London, Eastern Cape .

Key Responsibilities

• Perform a wide range of analytical tests on raw materials, intermediates, and finished products using various techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer titration).
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Calibrate, maintain, and troubleshoot laboratory equipment to ensure accurate and reliable results.
• Interpret analytical data, document results accurately, and prepare comprehensive reports.
• Investigate Out-of-Specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
• Ensure all laboratory activities are conducted in compliance with GMP, GLP, and relevant pharmacopoeial standards (e.g., USP, EP).
• Maintain accurate and detailed laboratory records and documentation.
• Participate in internal and external audits of the Quality Control laboratory.
• Assist in the training and mentoring of junior QC analysts.
• Stay current with advancements in analytical techniques and quality control methodologies.

Requirements

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• A minimum of 5-7 years of experience in pharmaceutical quality control laboratory operations.
• Proficiency in operating and maintaining common analytical instruments such as HPLC, GC, spectrophotometers, and dissolution apparatus.
• Strong understanding of GMP, GLP, and relevant pharmacopoeial requirements.
• Experience with analytical method development and validation is essential.
• Excellent data analysis, interpretation, and problem-solving skills.
• Meticulous attention to detail and a commitment to accuracy.
• Strong written and verbal communication skills.
• Ability to work effectively both independently and as part of a team.
• Familiarity with laboratory information management systems (LIMS) is a plus.

Benefits

• Our client offers a competitive salary, comprehensive medical aid, and a provident fund.
• Performance-based bonuses and opportunities for professional development, including advanced training and certifications, are provided.
• The company culture emphasizes quality, integrity, and teamwork, with a focus on employee growth and a positive work environment.
• Enjoy a healthy work-life balance and generous annual leave.
• This role offers a significant contribution to product quality assurance in the pharmaceutical industry, based in East London .