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RssSenior Scientist - M.S. Biologist, medical diagnostic industry, 20+ years experience. R&D, Manufacturing, Quality Assurance, Technical Support, and Quality Systems.

M.S. Biologist, molecular biology background, medical diagnostic industry. Experienced in R&D, Manufacturing, Quality Assurance, Technical Support, 21 CFR 820, audits, submissions and FDA communications. Proficient in technical reports, documentation, presentations, analytical instrumentation (HPLC, CE, UV-VIS), statistics (JMP, DOE, SPC, specifications), immunoassay development (ELISA, purification, conjugation), test method validations, 21 CFR 820 (cGMP)/ISO 13485, CAPA, change control, DMAIC investigations, risk management, ICH, GHTF, other standards/guidelines. Detailed, organized, thorough. Excellent communication skills (verbal/written). Valued team-member, individual contributor, and mentor. Make informed, critical decisions/minimal direction. Proven project management skills. Provide consistent, timely delivery of complex projects, effective/sustained on implementation. I maintain my professional skills as evidenced by obtaining the ASQ CQE, ASQ CQA, and a licensed Illinois pharmacy technician. Currently, I am attending graduate studies at Northwestern University for a MS in Clinical Research and Regulatory Adminiztration (CRRA). These attributes make me an ideal candidate for a diversity of challenging positions in the diagnostic and pharmaceutical industries. I am currently pursuing new opportunities. Please contact me for further discussion (224-545-6905).


Gurnee, IL

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Science & Biotech



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Gurnee, IL