Senior Analytical Chemist - Pharmaceutical Quality Control

Placements24; East London; Hybrid; ZAR 800,000 - 1,200,000; Full time

Benefits offered by this job

Competitive salary

Health and retirement benefits

Professional development opportunities

Generous paid time off

Quality-focused culture

Job summary

Placements24 in East London, Eastern Cape, is seeking a Senior Analytical Chemist to join its Quality Control team. The role focuses on developing, validating, and executing analytical methods to ensure the quality of pharmaceutical products, with hands-on work in the lab and data analysis in a hybrid setup.

You will work with HPLC, GC, UV-Vis, IR, and dissolution methods, ensure GMP compliance, and mentor junior staff.

Qualifications

• Bachelor’s or Master’s degree in Chemistry or a related field with hands-on pharmaceutical analytics experience.
• Minimum 5 years in analytical chemistry within the pharmaceutical industry.
• Strong hands-on experience with HPLC and GC systems and other instrumental techniques.
• Solid understanding of GMP and ICH guidelines and data interpretation.

Responsibilities

• Develop, validate, and transfer analytical methods for raw materials, in-process samples, and finished products.
• Perform routine testing using HPLC, GC, UV-Vis, IR, and dissolution methods.
• Analyze complex data and ensure compliance with specifications.
• Troubleshoot instrumentation and methods; implement corrective actions.
• Author and review method validation reports and SOPs; maintain documentation.

Skills

Analytical chemistry

Data analysis

Problem solving

Communication skills

Independent work

Education

Bachelor’s or Master’s degree in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

HPLC

GC

UV-Vis

IR spectroscopy

Dissolution testing

Job description

About the Role

Our client, a dynamic pharmaceutical company dedicated to advancing healthcare, is seeking a highly skilled Senior Analytical Chemist to join their Quality Control department in East London, Eastern Cape. This vital role involves developing, validating, and executing analytical methods to ensure the quality, purity, and potency of pharmaceutical products. You will utilize a range of advanced analytical techniques and play a key part in regulatory compliance and product release. The ideal candidate will possess a deep understanding of pharmaceutical analysis, regulatory guidelines (e.g., GMP, ICH), and extensive hands-on experience with analytical instrumentation. This position offers a stimulating work environment within our modern laboratory facilities in East London, with a hybrid work model allowing for focused lab work and remote data analysis and report writing.

Key Responsibilities

• Develop, validate, and transfer analytical methods for raw materials, in-process samples, and finished products.
• Perform routine testing of pharmaceutical samples using techniques such as HPLC, GC, UV-Vis, IR spectroscopy, and dissolution testing.
• Analyze and interpret complex analytical data, ensuring accuracy and compliance with specifications.
• Troubleshoot analytical instrumentation and methods, implementing corrective actions.
• Author and review analytical method validation reports, standard operating procedures (SOPs), and technical documentation.
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and relevant regulatory requirements.
• Collaborate with formulation development, manufacturing, and regulatory affairs departments.
• Maintain laboratory equipment and ensure proper calibration and maintenance schedules.
• Mentor junior analytical chemists and provide technical guidance.

Requirements

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in analytical chemistry within the pharmaceutical industry.
• Strong hands-on experience with various analytical instruments, particularly HPLC and GC systems.
• Thorough understanding of pharmaceutical quality control principles and GMP guidelines.
• Experience with method development and validation according to ICH guidelines.
• Proficiency in data analysis and interpretation, including statistical analysis.
• Excellent problem-solving skills and meticulous attention to detail.
• Strong written and verbal communication skills.
• Ability to work independently and manage multiple tasks effectively.

Benefits

• competitive salary commensurate with experience
• comprehensive health and retirement benefits
• opportunities for professional development and career advancement
• Employees enjoy generous paid time off
• supportive work culture focused on quality and innovation

Join our dedicated team in East London and be part of a company committed to improving patient lives.