Scientific. Clinical. Software Engineering
Job Description
Position Summary:
Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods.
Assists in the training of QC staff as needed.
Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software.
Writes and executes protocols and reports.
Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
Requirements:
flow cytometry and cell culture experience is preferred.
PCR experience is a plus.
bachelor + 5 years of experience or master degree is preferred.
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