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Associate Scientist

In Illinois / United States

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Associate Scientist   

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JOB TITLE:
Associate Scientist
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Abbott Park Illinois / United States

JOB DESCRIPTION :
Associate Scientist
Pay Rate: $25.06/HR

Cortech is seeking an Associate Scientist for our client in Abbott Park IL.


Job Description:
Support Reagent manufacturing. Conduct investigations on internal nonconformances and customer complaints related to Reagents. Assist in developing/ improving Reagent manufacturing processes and/or products.

Major Responsibilities:
--Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.
--Must demonstrate strong problem solving and analytical skills and be a team player.
--Must possess a BS in molecular biology, biochemistry, or related field with at least one to two years of relevant experience.
--Knowledge of GMP, ISO, and FDA regulations and audits a plus.
--Familiar with process and test method validations.
--Excellent communication skills.
--Shall be able to perform under pressure to meet project deadlines.

Position Details

Jun 19, 2021
Health Care
S16204860651322160
Illinois / United States
Abbott Park
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Associate Scientist    Apply

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Associate Scientist
Pay Rate: $25.06/HR

Cortech is seeking an Associate Scientist for our client in Abbott Park IL.


Job Description:
Support Reagent manufacturing. Conduct investigations on internal nonconformances and customer complaints related to Reagents. Assist in developing/ improving Reagent manufacturing processes and/or products.

Major Responsibilities:
--Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.
--Must demonstrate strong problem solving and analytical skills and be a team player.
--Must possess a BS in molecular biology, biochemistry, or related field with at least one to two years of relevant experience.
--Knowledge of GMP, ISO, and FDA regulations and audits a plus.
--Familiar with process and test method validations.
--Excellent communication skills.
--Shall be able to perform under pressure to meet project deadlines.