Associate Scientist
Company: Planet Pharma
Location: New Haven
Posted on: November 27, 2025
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Job Description:
Job Description You will be responsible for: Accurately,
capture, verify and standardize assay performance data across
platforms to support method performance evaluation across global
testing network. Interface with laboratory teams, refine data
pipelines, enhance metadata standards, and drive continuous
improvements in assay trending workflows. Produce clear summaries,
dashboards, periodic reports for stakeholders and help support SOP
updates. Support analytical data verification for assay performance
and analytical transfer/validation reports for late stage clinical
and commercial programs. Contribute to analytical method
evaluation, as needed, in the laboratory. You will need to have:
Strong hands-on experience in the development and execution of
analytical methods for biological products, especially in cGMP
environment, is a significant plus. Ability to conduct critical
evaluation of scientific documentation and testing data. Excellent
written and verbal communication skills. Excellent collaboration
skills and experience working in cross functional teams. Strong
familiarization of cGMP regulations pertaining to analytical
testing, validation and transfer, and expertise in analytical
laboratories. Excellent organizational skills, attention to
details, creative thinker and complex problem solver. Work
comfortably in a controlled environment with biological,
infectious, and hazardous materials under PPE. The duties of this
role are conducted in a lab environment. As is typical of a
lab-based role, employees must be able, with or without an
accommodation to: lift/carry 15/30 pounds unassisted/assisted ;
work comfortably in a controlled environment with and around
biological, infectious, and hazardous materials; gown/degown PPE;
use a computer; engage in communications via phone, video, and
electronic messaging; engage in problem solving and non-linear
thought, analysis, and dialogue; collaborate with others; maintain
general availability during standard business hours. We would
prefer for you to have: Bachelor’s or master’s degree in chemistry,
Biochemistry, Molecular and Cell Biology or related discipline. 3-6
years of experience working in a relevant analytical laboratory
setting. Experience with JMP, electronic documentation and quality
management systems. Strong hands-on experience in cGMP environment.
Experience working in fast-paced team environment. High level of
proficiency in MS Office software including Word, Excel, Outlook,
Visio, and PowerPoint.
Keywords: Planet Pharma, New Haven , Associate Scientist, Science, Research & Development , New Haven, Connecticut
