Job description

Requirements

  • Entry level
  • No Education
  • Salary CHF80,000.00 - CHF100,000.00 gross per year
  • Basel

Description

- Plan and carry-out analytical tests according to current good manufacturing practices (cGMP) standards on drug products in clinical development or commercial phase (specifically focused on HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visible particles, subvisible particles and related DP analytics)
- Contribute to planning of analytical method validation as well as execute and evaluate validation experiments
- Support cGMP regulated analytical method transfer
- Ensure proper maintenance of equipment, safety and health protection following lab and safety instructions and all cGMP regulations
- Install, qualify and maintain instruments according to best practices and regulations
- Support establishment of DP analytical infrastructure and services for biologics, small molecule and peptide parenteral products for clinical and commercial products


- Completed vocational training as BTA, PTA, CTA or equivalent or a degree as B.Sc. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related subject
- Extensive working experience as a technical assistant in the pharmaceutical or chemical industry, preferably in analytics
- Strong working knowledge in majority of relevant analytical techniques
- Very good reporting, interpretation and documentation skills of scientific results
- Good knowledge of written and spoken English
- Experience working in a cGMP-regulated environment is advantageous
- Proficiency in development of parenteral dosage forms and protein analytics is beneficial

  • scientists and researchers