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Premier Medical USA Corporation
Somerset, NJ
Start date
Apr 30, 2024

Job Details

Responsibilities include working with scientists on standard data analysis and communicate the results to team, analyze and troubleshoot technical issues related to protocol development and quality for immunodiagnostics products.

Design and Development of recombinant antigens and antibodies. Preparation of technical documents for ISO 13485:2016 and 21 CFR part 820.

Conduct experiments to evaluate the performance of immunodiagnostics products.

Interact with internal departments to plan and expedite project objectives.

Prepare regular reports documenting experimental results.

Follow quality system of ISO 13485:2016, clause 7.3 for design and development.


40 hrs./wk. M-F.

Master’s Degree in Microbiology with 2 years of professional experience and have practical knowledge of ISO 13485:2016


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