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Associate Scientist I

In California / United States

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Associate Scientist I   

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JOB TITLE:

Associate Scientist I

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Carlsbad California / United States

JOB DESCRIPTION:

This position is NonExempt. Hours over 40 will be paid at Time and a Half. 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

POSTED:

Apr 17, 2022

EMPLOYMENT:

INDUSTRY:

Health Care

SNAPRECRUIT ID:

S164386080767151

LOCATION:

California / United States

CITY:

Carlsbad

Job Origin:

Jobsrus_organic_feed

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Associate Scientist I    Apply

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This position is NonExempt. Hours over 40 will be paid at Time and a Half. 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.


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