Associate Scientist II- Immunoassay

ResolianMalvern, AR
103d

About The Position

This position involves a variety of responsibilities centered around laboratory work, including the preparation of reagents, standards, and control samples, as well as the analysis of samples using various techniques specific to the department. The role requires assisting with method development and performing method validation or qualification. The candidate will operate analytical equipment, lead troubleshooting activities, and maintain the analytical equipment to ensure it is in optimal working condition. Additionally, the candidate will be responsible for keeping the lab area clean and inspection-ready at all times, removing lab waste, and recording tasks in accordance with Good Documentation Practices (GDP). Understanding and applying regulatory requirements such as GLP, GCP, and 21CFR Part 11 is essential, along with following applicable SOPs and procedural documents. The role also includes reviewing and evaluating data results, training lower-level scientists, and performing other tasks as assigned.

Requirements

  • BA/BS or higher with 4-6 years lab experience; all experiences will be evaluated
  • Able to perform complex lab work
  • Experience working in a regulated environment
  • CRO experience preferred
  • ELISA, MSD experience or pipetting efficiency needed
  • Ligand binding/ immunoassay experience
  • Able to work effectively and contribute within a team
  • Able to work with computer systems
  • Able to document clearly; Knowledge of and experience in a regulatory environment

Responsibilities

  • Prepare reagents, standards, and control samples
  • Analyze samples using various techniques specific to department
  • Assist with method development
  • Perform method validation or qualification
  • Operate analytical equipment
  • Lead troubleshooting activities
  • Maintain analytical equipment
  • Ensure lab area is clean and inspection ready at all times
  • Remove lab waste
  • Record tasks in accordance with Good Documentation Practices (GDP)
  • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11
  • Follow applicable SOPs and procedural documents
  • Review and evaluate data results
  • Train lower level Scientists
  • Other tasks as assigned
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