- We offer a position in the Pharmaceutical Chemical Analysis Department as a Scientist responsible for the analysis of active ingredients and pharmaceutical specialties.
- The role involves designing, supervising, and conducting studies on the development and validation of analytical methods for drug control, stability studies, quality control, etc. Analytical techniques employed include HPLC, GC, potentiometry, Karl Fisher, UV, dissolution testing, etc.
- The work is conducted in compliance with GLP and GMP regulations.
- We are seeking an individual with a Bachelor's degree in Chemical Sciences (Analytical Orientation). A Ph.D. is highly valued.
- The ideal candidate has some knowledge in HPLC, GC techniques, and have a basic understanding of an analytical development department.
- Some experience in the development and validation of new analytical methods for quality control of pharmaceuticals is valued.
- Previous experience in chemical analysis of active ingredients and pharmaceutical formulations in a Quality Control or Analytical Development department of a pharmaceutical or related company is preferred.
- Experience working with GLP and GMP is required.
- Minimum English language proficiency level: First Certificate.
- Availability for morning shift (6pm-14pm).
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Quality Control Scientist - Cerdanyola del Vallès, España - Kymos
Descripción
Kymos is hiring a Scientist in Chemical Analysis for our Quality Control department:
Position Description:
Profile of the required person:
