Executive Job Title	Medical Diagnostics Principal Consultant
Type of Registrant	Recruiter
Location	Washington DC
Industry & Function 1:	Biotechnology - R&D-Research-Management
Industry & Function 2:	Consulting--Management--(alsoEngineering/Science) - CONSULTANT-/-R&D-Management-of-Research
Industry & Function 3:	Pharmaceuticals(Ethical)/Surgical/Medical-Equip. - R&D-Research-Management
Compensation	$100,000 to $200,000
Executive Job Description	Our client is a prestigious consulting firm with a business unit focusing on the life sciences industry and government agencies markets They provide technical, regulatory, manufacturing and operational improvement services across the entire pharmaceutical/biopharmaceutical industry from discovery through commercialization. Approximately 5 years ago they added consulting offering within the critical life science and biomedical R&D segments of the federal government. As pandemic disease preparedness and bioterrorism became ever more critical issues, our client has increasingly worked with the Department of Homeland Security and Department of Defense. This role will offer a significant exposure to other high-level individuals both within private industry and the US Federal Government which will prove highly valuable to your future career. What you will need: A MS (PhD. preferred) in immunology, molecular biology, engineering or similar scientific discipline and l5+ years of experience developing or manufacturing molecular or immunologic diagnostics components or systems. This includes current Best-Manufacturing-Practices knowledge and deep expertise in reagent or device development, familiarity with manufacturing processes associated with rare reagents, monoclonal antibodies or diagnostic devices. Additionally, your background should include experience in identifying and resolving regulatory and manufacturing technical problems; Knowledge of routine analytical methods; Ability to determine the most appropriate methodology for the validation of the manufacturing process; with a good understanding of CDRH regulatory hurdles.
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