CTC Clinical Trial Consulting AG C

Associate Scientist Analytical Development & QC (BB-2CAA4)

Gefunden in: Xpatjobs CH

Main Responsibilities: Development, optimization and application of analytical methods ( 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 through compilation of all analytical testing records (e.g.notebooks, raw data hardcopies).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 workspace. Qualifications and Experience: Relevant working/residency permit or Swiss/EU-Citizenship required.Apprenticeship/ College/ University degrees or equivalent education in the field of chemistry, biology,biochemistry, pharmacy, or chemical engineeringApprenticeship 4-6 years, BS 2-4 years or MS 1-3 years experienceAbility to efficiently plan and effectively execute and document analytical experiments in a GMP-compliant pharmaceutical environmentBasic knowledge of GMPGood knowledge of sample preparation, HPLC instrumentation and techniquesBasic knowledge of spectroscopic methods, e.g., UV/VIS, IRBasic trouble-shooting skills for analytical analyses

calendar_todayvor 3 Tagen


location_on Basel , Basel-Stadt, Schweiz

work CTC Clinical Trial Consulting AG

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