Scientific Associate ADQC

Main Responsibilities :

• Development, optimization and application of analytical methods, e.g., for purity-, stability-,
• content-and potentially genotoxic impurity determinations.
• Write-up of analytical methods for implementation.
• Conduct of release, retest, stability studies, transfer and validation analyses.
• Proper documentation of all analytical activities according to Good Documentation Practices
• Interpretation and documentation of analytical data including results from method development,
• release, retest, validation, stability, and transfer.
• Write-up of analytical protocols and reports, e.g., for validation and stability studies.
• Assurance of adequate maintenance and operation of analytical equipment according to GMP.
• Drafting and review of CoAs and / or Analytical results sheet.
• Drafting of SOPs, GUIs, TPLs, FRMs.
• Training of Laboratory personnel.
• Ensuring of cleanliness of laboratory and work space.

Qualifications and Experience :

• Relevant Swiss working / residency permit and / or Swiss / EU-Citizenship required;
• Apprenticeship-, College-, or university-degree or equivalent education in the field of chemistry, biology, biochemistry, pharmacy, or chemical engineering with apprenticeship 4-6 years, 2-4 years BS or 1-3 years MS experience.
• Ability to efficiently plan and effectively execute and document analytical experiments in a GMP-compliant pharmaceutical environment.
• Basic knowledge of GMP. Good knowledge of sample preparation, HPLC instrumentation and techniques.
• Basic knowledge of spectroscopic methods, e.g., UV / VIS, IR. Basic trouble-shooting skills for analytical analyses.
• Flexibility, good communication, time management and team-working skills.
• Ability to work independently and to take initiative. Life-long learning mindset.
• Proficient in English

If you'd like to learn more about CTC and the outlined opportunity, please contact us using the 'apply now' button or by emailing [email protected]