Scientific Associate ADQC
CTC Resourcing Solutions
- Bâle
- Contrat
- Temps-plein
- 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.
- 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