Quality Control Analyst performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conducts and validates various biological and chemical quality control (QC) assays. Being a Quality Control Analyst compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. May be responsible for establishing specifications for conducting assays and writing standard operating procedures. Additionally, Quality Control Analyst typically requires a bachelor's degree. Typically reports to a supervisor or manager. The Quality Control Analyst work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Quality Control Analyst typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)
Johnson & Johnson Family of Companies
Title: Laboratory Technical Writer
Location: Raritan, NJ - 100% Onsite
Duration: 1 year
Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits
Please note that this is a contract role providing services to the Johnson & Johnson Family of Companies through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be a member of the Johnson & Johnson Family of Companies.
Summary:
The Technical Writer will plan, execute, and write laboratory investigations/deviations, in coordination with laboratory leads, identifying assignable/root causes and determining effective corrective and preventative actions.
Responsibilities:
Qualifications:
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0 Quality Control Analyst jobs found in Somerset, NJ area