Scientific Associate
RBW Consulting
- Allschwil, Bâle-Campagne
- Contrat
- Temps-plein
- Method Development: Lead the development, optimization, and application of analytical methods, including purity, stability, content, and potential genotoxic impurity determinations.
- Documentation: Write up analytical methods for implementation and ensure proper documentation of all analytical activities according to Good Documentation Practices.
- Study Conduct: Conduct release, retest, stability studies, transfer, and validation analyses in compliance with GMP and regulatory guidelines.
- Data Interpretation: Interpret and document analytical data from various stages including method development, release, retest, validation, stability, and transfer.
- Reporting: Write up analytical protocols and reports for validation and stability studies.
- Equipment Maintenance: Ensure adequate maintenance and operation of analytical equipment according to GMP standards.
- Compliance: Draft and review Certificates of Analysis (CoAs), Analytical Results Sheets, SOPs, GUIs, TPLs, and FRMs.
- Training: Provide training to laboratory personnel and ensure cleanliness of the laboratory and workspace.
- Degree or apprenticeship in relevant life sciences subject.
- Circa 2 years+ work experience in an analytical laboratory.
- Basic knowledge of GMP Proficiency in sample preparation, HPLC instrumentation, and techniques.
- Familiarity with spectroscopic methods such as UV/VIS, IR, and basic troubleshooting skills for analytical analyses.
- Strong communication, time management, and team-working skills.
- Proficient in English.
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