Location
Pathum Thani, Thailand
Salary
Not specified
Type
fulltime
Posted
Today
via linkedin
Job Description
Job Resposibilities:
- Design and author clinical protocols for in vivo skin penetration studies
- Prepare and submit Human Research Ethics Committee (EC/IRB) applications; manage volunteer recruitment, screening, and informed consent
- Operate the CRS system: depth profiling, spectral acquisition, optical alignment, laser safety
- Acquire and validate reference spectra for SRL actives, maintain the spectral reference library, and review depthprofile outputs for fit quality and artefacts.
- Write SOPs, validation protocols, and uncertainty budgets to ISO/IEC 17025 standards
- Produce clientfacing technical reports and support technical discussions with international customers
- Correlate in vivo CRS results with in vitro methods (Franz cell, tape stripping) and other skin biophysics endpoints
Qualification:
- Master of Science with 2–5 years relevant hands-on experience, or PhD with 1-3 years, in Pharmaceutical Sciences/Pharmaceutics, Analytical Chemistry, Physics/Biophysics, Biomedical Science, Cosmetic Science, or a related field
- Comfort with spectral data — baseline correction, normalisation, and interpretation of fitted component profiles.
- Humansubjectresearch experience — protocol writing, EC/IRB submission in Thailand, Thai language consent and volunteer briefing, randomisation and blinding, sourcedata discipline. ICHGCP training strongly preferred.
- Skin science fundamentals — stratum corneum structure, the SC water gradient and natural moisturising factor, partition and diffusion principles, and the distinction between penetration, permeation, and systemic absorption.
- Qualitysystem discipline — SOP authoring, method validation, measurement unce
- Good command in English both speaking and writing
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