Analytical Development Scientist - Pharmaceutical Analysis

Placements24; East London; On-site; ZAR 600,000 - 900,000; Full time

Job summary

Placements24 seeks an Analytical Development Scientist to join its Quality Control and Assurance team in East London. The role develops, validates, and implements analytical methods for raw materials, in-process samples, and finished products.

You will work with HPLC, GC, UV-Vis, dissolution, and Karl Fischer techniques, ensuring GMP/GLP and ICH compliance. A 3-year pharma background and strong data analysis and writing skills are essential.

Qualifications

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
• Minimum 3 years of experience in analytical development or quality control within the pharmaceutical industry.
• Proficiency with analytical instrumentation, especially HPLC and GC.
• Strong understanding of method validation principles and regulatory requirements (ICH).
• Excellent data analysis, problem solving, and technical writing skills.
• Ability to work independently and as part of a team in East London.

Responsibilities

• Develop, optimize, and validate analytical methods for QC and materials.
• Perform routine and non-routine analytical testing using HPLC, GC, UV-Vis, dissolution, and Karl Fischer.
• Investigate and troubleshoot analytical method issues and OOS results.
• Prepare method validation reports, analytical specifications, and SOPs.
• Collaborate with formulation, manufacturing, and regulatory teams to support product development and release.
• Ensure all laboratory activities are conducted in compliance with GMP, GLP, and relevant regulatory guidelines.

Skills

HPLC

GC

UV-Vis

Dissolution

Karl Fischer

Data analysis

Technical writing

Teamwork

Problem solving

Independent work

Education

Bachelor's/Master's in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

HPLC systems

GC systems

Job description

About the Role

Our client is seeking a skilled and motivated Analytical Development Scientist to join their Quality Control and Assurance department in East London . This role is crucial for developing, validating, and implementing analytical methods used to test raw materials, in-process samples, and finished pharmaceutical products. You will play a key role in ensuring product quality and compliance with regulatory standards through robust analytical testing and characterization. The ideal candidate will possess strong expertise in various analytical techniques and a commitment to scientific rigor within the pharmaceutical industry.

Key Responsibilities

• Develop, optimize, and validate analytical methods for the characterization and quality control of pharmaceutical products and raw materials.
• Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, dissolution, and Karl Fischer titration.
• Investigate and troubleshoot analytical method issues and out-of-specification (OOS) results.
• Prepare method validation reports, analytical specifications, and standard operating procedures (SOPs).
• Collaborate with formulation, manufacturing, and regulatory teams to support product development and release.
• Ensure all laboratory activities are conducted in compliance with GMP, GLP, and relevant regulatory guidelines.

Requirements

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 3 years of experience in analytical development or quality control within the pharmaceutical industry .
• Proficiency with analytical instrumentation, particularly HPLC and GC systems.
• Strong understanding of method validation principles and regulatory requirements (e.g., ICH guidelines).
• Excellent data analysis, problem-solving, and technical writing skills.
• Ability to work independently and as part of a team in a laboratory setting in East London .

Benefits

• Competitive salary and comprehensive benefits package.
• Opportunity to work with advanced analytical technologies and contribute to product quality.
• Generous paid time off and retirement savings plan.
• Support for professional development and continuing education.
• A collaborative work environment focused on scientific excellence and regulatory compliance.