Pharma Analytical R&D Executive – Method Development

Duopharma Biotech Bhd Group of Companies.

Shah Alam

Vor Ort

MYR 72.000 - 110.000

Vollzeit

Vor 13 Tagen

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Zusammenfassung

Duopharma Innovation Sdn. Bhd. is seeking an Executive, Analytical to join the Analytical Department in Glenmarie, Selangor.

The role focuses on developing and validating analytical methods, conducting stability studies, and supporting pharmaceutical product development under GLP and ISO/IEC 17025 standards. You will collaborate with Formulation, Quality Management, Production, and Quality Control teams to ensure reliable testing, cross-functional support during scale-up, and timely regulatory

Qualifikationen

  • Bachelor's Degree in Science or a related discipline.
  • Minimum 3 years of experience in pharmaceutical or related industry.
  • Experience in analytical laboratory operations or similar capacity.

Aufgaben

  • Develop and validate analytical methods for raw materials, active ingredients, intermediates, and finished products.
  • Perform analytical testing using HPLC, GC, MS, ICP-OES, and other instruments.
  • Conduct stability study testing for R&D batches.
  • Support product development, technology transfer, and regulatory submissions.
  • Prepare and maintain analytical documentation (Lab notebooks, development reports, SOPs).

Kenntnisse

Analytical method development
GLP
Regulatory knowledge
Teamwork & communication

Ausbildung

Bachelor's degree in Science or related

Tools

HPLC
GC
MS
ICP-OES
Dissolution Testing
UV-Vis Spectrophotometer

Jobbeschreibung

Duopharma Innovation Sdn. Bhd. is seeking an Executive, Analytical to join the Analytical Department in Glenmarie, Selangor.

The role focuses on developing and validating analytical methods, conducting stability studies, and supporting pharmaceutical product development under GLP and ISO/IEC 17025 standards. You will collaborate with Formulation, Quality Management, Production, and Quality Control teams to ensure reliable testing, cross-functional support during scale-up, and timely regulatory

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