Research Associate, Analytical Development
Full-timeMidAnalytical DevelopmentBiologicsUnknownBachelors
Description
The Research Associate, Analytical Development will be responsible for executing the development / implementation / optimization of assays necessary for assessing protein characteristics. Another key responsibility is to execute routine execution of platform tests necessary to assess the quality of manufactured lots and to support discovery and process development activities. Additional responsibilities will be to participate in the pre-validation of developed assays, using defined scientific and regulatory practices, to perform the trending of data, and to write and/or review analytical documentation. The incumbent will also participate in the development of product formulation studies and stability studies. Key Responsibilities include:
- Analyze recombinant protein candidates produced from mammalian cells using typical assays for protein characterization (e.g.: HPLC, CE, SDS-PAGE, DLS, ELISA).
- Execute the implementation of analytical assays for R&D purposes as well as for transfer to quality control laboratories.
- Participate in the design and execution of product stability studies.
- Analyze experimental data and properly document experiments (electronic lab notebook and records).
- Participate in the development of protein formulation chemistry and the execution of required analyses.
- Generate protocols and reports on performed experiments.
- Perform routine laboratory equipment maintenance.
- Participate in technology transfer activities, as required.
Requirements
- At a minimum, an undergraduate level (B.Sc.) in biochemistry, biotechnology, life sciences or equivalent.
- At least 3 years of experience in the performance of analyses including data interpretation on proteins.
- Experienced with at least one of these types of analyses: HPLC, Capillary Electrophoresis (CE), Dynamic Light Scattering (DLS), and immunological techniques (ELISA).
- Track record demonstrating to be meticulous and detail oriented.
- Knowledge of analytical technologies for proteins.
- Knowledge of the current Good Manufacturing Practices (cGMP) is an asset.
35Pharma
PHARMACEUTICAL
Ligand Traps for Diseases of High Unmet Medical Need
LocationQC - Montreal
Open Jobs8
Rare Diseases
View Company ProfilePipeline
CON . control condition without exercise / rest conditionN/A
CON . control condition without exercise / rest conditionN/A
DEF-EI : Energy restriction induced energy deficitN/A
HS235Phase 1
HS235Phase 1