Follow operating procedures to test and deliver reports on products in a fast paced environment with constantly changing priorities and deadlines.Responsibilities include: assisting regulatory in providing test reports, summaries, justifications, and AI responses for the FDA. Ensuring compliance in a quality controlled lab (GDP, GLP, GMP, CFR), writing SOPs based of various standard bodies (ASTM, ISO, BS EN, etc.), validations (IQOQPQ, Equipment, Product, and spreadsheet), designing and performing studies designed for market research and 510k submissions, working across internal and external teams to implement new products into market. Utilizing CAPAs to improve processes. Identifying deviations to SOPs and conducting investigations. Performing GAP analysis on standards when a new revision is published.