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Scientific Associate Adqc
vor 3 Monaten
Our client, an innovative Swiss bio-pharmaceutical company, is seeking an
Scientific Associate in Analytical Development for a 12-month contract in the Basel area.
Main Responsibilities:
- content-and potentially genotoxic impurity determinations.
- Writeup 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,
- Writeup 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:
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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 GMPcompliant 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 troubleshooting skills for analytical analyses.
- Flexibility, good communication, time management and teamworking skills.
- Ability to work independently and to take initiative. Lifelong learning mindset.
- Proficient in English