Scientist Analytical Development (cGMP)

  • New Haven, CT
  • Posted 8 hours ago | Updated 8 hours ago

Overview

On Site
$35 - $38
Full Time

Skills

Analytical Skill
Assays
Biochemistry
Chemistry
JMP
Meta-data Management
Quality Control
Documentation
Quality Management
Good Manufacturing Practice
Cell Biology

Job Details

Title: Associate Scientist III Analytical Development & QC (Onsite New Haven, CT)
The client is seeking an Associate Scientist III to support analytical development and quality control activities across early to late-stage clinical programs. This role is 100% onsite in New Haven, CT and requires strong collaboration with internal and external QC labs to support assay performance trending and analytical method evaluation.

Key Responsibilities:
Capture, verify, and standardize assay performance data across platforms
Partner with QC labs to refine data pipelines and enhance metadata standards
Prepare dashboards, summaries, and periodic analytical reports
Support analytical data verification for method transfer/validation
Contribute to method evaluation activities in the lab

Requirements:
3 6+ years of analytical lab experience (biologics preferred)
Strong hands-on experience in cGMP analytical environments
Ability to interpret scientific data and documentation
Proficiency in MS Office; experience with JMP and electronic quality systems a plus
Excellent communication, attention to detail, and organizational skills
Ability to work in lab environment with biological/hazardous materials

Education:
Bachelor s or Master s in Chemistry, Biochemistry, Molecular/Cell Biology, or related field

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