Senior Analytical Development Scientist -cGMP (East London)

Placements24; East London; Vor Ort; ZAR 900.000 - 1.200.000; Vollzeit

Benefits dieser Stelle

Medical aid

Pension fund

Paid annual leave

Professional development

State-of-the-art lab facilities

Zusammenfassung

Placements24 is seeking a Senior Analytical Development Scientist in East London, Eastern Cape, SA to lead method development and validation for pharmaceutical products. You will perform hands-on laboratory work and ensure cGMP compliance across projects from early development to commercial support.

The role requires a strong background in analytical chemistry, extensive experience with HPLC/UPLC, GC and spectroscopy, and collaboration with QA, QC and R&D teams.

Qualifikationen

• Minimum of 5 years of experience in analytical method development and validation within the pharmaceutical industry.
• Knowledge of cGMP regulations and ICH guidelines related to analytical testing and validation.
• Strong problem-solving, analytical and organizational skills.
• Excellent written and verbal communication skills.

Aufgaben

• Develop, optimize, and validate analytical methods for raw materials, intermediates and finished products.
• Perform routine testing using HPLC, GC, UV-Vis, FTIR and dissolution methods.
• Characterize drug substances and products, including impurity profiling and stability testing.
• Troubleshoot analytical methods and instrumentation issues.
• Prepare development reports, validation protocols and validation reports.
• Ensure regulatory compliance with cGMP and guidelines; support regulatory submissions.
• Collaborate with Quality Control, QA and R&D teams.
• Maintain and calibrate laboratory equipment and instruments.

Kenntnisse

Analytical chemistry

Method development

Method validation

Regulatory knowledge

Ausbildung

Master's or PhD in Analytical Chemistry or Pharmaceutical Sciences

Tools

HPLC

UPLC

GC

MS

UV-Vis

FTIR

Jobbeschreibung

Placements24 is seeking a Senior Analytical Development Scientist in East London, Eastern Cape, SA to lead method development and validation for pharmaceutical products. You will perform hands-on laboratory work and ensure cGMP compliance across projects from early development to commercial support.

The role requires a strong background in analytical chemistry, extensive experience with HPLC/UPLC, GC and spectroscopy, and collaboration with QA, QC and R&D teams.