Archiviertes Projekt - Quality Control Analyst (m/f/d)
Firmenname für PREMIUM-Mitglieder sichtbar
- August 2024
- nicht angegeben
- CH-Bern
- auf Anfrage
- 12.07.2024
- 772493/1-en
Projektbeschreibung
Ihre Aufgaben:
• Responsible for the management and delivery of small projects and project deliverables
• Development, optimization, and/or validation of methods specific to biochemistry
• Responsible for the development of experimental plans, including estimating materials, resources, and times required for identified work
• Execute appropriate testing and experimental plans as required
• Author, review, and update protocols, reports, test procedures, and associated documentation in the performance of experimental studies
• Contribute to the subject matter expertise during the investigation of deviations, atypical results, and method performance issues
• Active participation in project meetings and regulatory submissions as required
• Ensure timely communication and completion of deliverables, while working in accordance with cGMP and data integrity principles
Ihre Qualifikationen:
• Master's Degree in Biological Science or other appropriate technical field. Doctoral degree is preferred or the equivalent industry experience
• Solid experience in method development/validation for assessment of biological pharmaceutical products, or equivalent post-graduate experience
• Experience in cGMP Quality Control is a plus
• Strong experience in immunoassays, cell-based assays and electrophoretic techniques
• Proven written and verbal communication skills
• Excellent knowledge of English and German
• Ability to operate independently and as part of a team
Ihre Vorteile:
• A highly motivated team and an open way of communication
• A very renowned company
Projektdauer: 12 MM
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
• Responsible for the management and delivery of small projects and project deliverables
• Development, optimization, and/or validation of methods specific to biochemistry
• Responsible for the development of experimental plans, including estimating materials, resources, and times required for identified work
• Execute appropriate testing and experimental plans as required
• Author, review, and update protocols, reports, test procedures, and associated documentation in the performance of experimental studies
• Contribute to the subject matter expertise during the investigation of deviations, atypical results, and method performance issues
• Active participation in project meetings and regulatory submissions as required
• Ensure timely communication and completion of deliverables, while working in accordance with cGMP and data integrity principles
Ihre Qualifikationen:
• Master's Degree in Biological Science or other appropriate technical field. Doctoral degree is preferred or the equivalent industry experience
• Solid experience in method development/validation for assessment of biological pharmaceutical products, or equivalent post-graduate experience
• Experience in cGMP Quality Control is a plus
• Strong experience in immunoassays, cell-based assays and electrophoretic techniques
• Proven written and verbal communication skills
• Excellent knowledge of English and German
• Ability to operate independently and as part of a team
Ihre Vorteile:
• A highly motivated team and an open way of communication
• A very renowned company
Projektdauer: 12 MM
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
Kontaktdaten
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Kategorien und Skills
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