Adriana Becker

US Regulatory Affairs Expert

Adriana Becker, MSc.
Regulatory Affairs Consultant

As part of the Regulatory Affairs Group, Adriana works with a variety of low/ high-risk devices under the EU MDR.

Before joining Qserve, she worked in Regulatory Affairs at Medtronic and Oasis Medical, gaining valuable experience with Class I-III devices under EU medical device (MDD) regulation, as well as across various emerging markets. Adriana started her career as a Quality Control Chemist at a multinational biopharmaceutical firm, Grifols Inc., and was later a part of their Diagnostic division, which develops diagnostic products in areas such as immunohematology, hemostasis, parasitology, immunology and blood transfusion.

Adriana holds degrees in Biochemistry (BSc) from Seton Hall University and Regulatory Science (MSc) from University of Southern California. With her BSc, she also obtained a secondary major in English Literature, which included extensive writing classes in topics such as Scientific and Technical Writing. She is of Romanian nationality and is fluent in Romanian and English, with developing professional fluency in French.

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