Research Officer Quality Control (Physical Chemistry Analyst) Temporary (9 months)

작업 내용

Research Officer Quality Control

(Physical Chemistry Analyst)

Temporary (9 months)

POSITION OVERVIEW:

For this 9 month temporary assignment, we are looking for highly motivated people who thrive on being challenged and working in an agile, collaborative, and multicultural environment to join our multidisciplinary Quality Control team and play a key role in conducting rigorous, cutting-edge science.

To partake in execution and enrichment of our ambitious pipeline of projects, this Research officer position is to be filled by an analytical scientist with a thorough understanding of GMP principles.

She or he will work together with the QC team on the analysis and characterization of biologics.

RESPONSIBILITIES:

• Perform routine analytical testing using the following methods: iCE, cGE, HLPC/UPLC, UV Vis, Solo VPE, pH, conductivity…) for batch release, stability testing and product characterization.
• Perform general lab tasks (ordering materials, maintaining inventory, preparing buffers, cleaning…).
• Comply with GMP requirements, adherence to data integrity principles at all time and apply all QC procedures.
• Complete documentation in a timely manner, prepare/review are documentation (SOPs, Protocols, reports…).
• Ensure training compliance within the assigned work area.
• Responsible for calibration, use and maintenance of laboratory instruments and equipment.
• Provide support and execute method troubleshooting.
• Report any non-conformances to Senior Research Officer/Management and assist in documentation.
• Identify and facilitate problem-solving and improvement projects.
• When needed, support method transfers and validation.
• Perform other relevant duties as required.

EDUCATION AND DESIRED EXPERIENCE:

• MSc or BSc in analytical sciences, biochemistry, biology, or biotechnology with 1-2 year’s relevant experience.
• Biotechnology industry experience is preferred.
• Hands on experience with protein characterization using liquid chromatography (RP-HPLC, SEC, ion exchange, etc...) and capillary electrophoresis.
• Ability to run experience in an autonomous manner. Critical thinking, good problem solving and analytical skills.
• Knowledge and experience in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) is an asset.
• Good organizational skills. Hands-on approach. Ability to work under time constrains and adapt to work schedule changes.
• Ability to work independently as well as part of a team.
• Ability to achieve and maintain high standards with meticulous attention to details.
• Fluency in English, both written and verbal; French is a plus

LOCATION:

You will join us, in a picturesque city of La Chaux-de-Fonds, Neuchâtel, Switzerland.

This is a rare opportunity to join our growing scientific team at the very start of something special. You will become a part of the foundation of a new company imprint…