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Associate Scientist

Cambridge, MA
Top 3 Must Have Skill Sets:    
  • (HANDS ON) HPLC expertise - able to operate, process data, and report findings into electronic lab notebook. (1+ years of experience)
  • Good documentation practices - bonus would be GMP/QC experience (1+ years of experience)
  • experience with participle detection methods (1+ years of experience)

soft skills
  • Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently.

Day to Day Responsibilities:    

Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance.

Summary:

To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 

Responsibilities include: 
  • Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision 
  • Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data 
  • Effectively transfers experimental methods from literature to the lab and makes modifications as necessary 
  • Develops and implements new protocols with moderate review 
  • Engages coworkers in scientific discussions 
  • Communicates data and interpretation to work group 
  • Skilled at developing systems to ensure quality data 
  • Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques 
  • Effectively trouble-shoots equipment and experimental difficulties 
  • Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents 
  • Participates in department-wide support efforts such as safety, recruiting and committees 
  • May train staff and/or supervise others 
  • Coordinates and organizes resources needed to complete the task 
  • Understands when to seek input and when to make independent judgments

Skills: 
  • degree in Biology, Biochemistry or Analytical Chemistry 
  • experience in a Biopharmaceutical working environment

Education: Bachelor Degree REQUIRED

"This posting is for Contingent Worker, not an FTE"

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