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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug discovery and development, cell and molecular biology, genetics, biochemistry, microbiology, laboratory instruction, biotechnology finance, regulatory affairs, clinical trials, project management, or manufacturing.
$3,527 a monthPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support Danaher Diagnostic Operating Company Medical and Scientific Affairs and Government Affairs organizations on their strategy so that it maximizes patient impact at scale. Prior roles in industry Medical and Scientific Affairs and/or Government Affairs functions a plus.
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Join the fastest growing outpatient radiology practice in the Nation- SimonMed Imaging! At SimonMed Imaging, we offer medical, vision and dental insurance, significant Imaging discounts, 401(k) eligibility, paid holidays plus PTO, Sick Time, opportunity for growth, and much more.
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Basic understanding of regulatory affairs concepts, guidelines, and regulations governing the development, documentation, and labeling of in vitro diagnostic products. Kelly® Science & Clinical is currently recruiting for a Technical Writer for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology realm.
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Hands-on experience with NGS and DNA/RNA molecular biology is required. Advanced degree in a scientific discipline with a strong background in molecular and cell biology, biotechnology, or biochemistry is required.
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Responsibilities: The successful candidate will decipher regulatory mechanisms in bacteria by combining global genome-wide methods (RNAseq) with the molecular analysis. Experience with other molecular biology techniques (e.g., Nucleic acids purification, vector constructions, PCR/RT-PCR amplification would be a plus.
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Provides imaging services as defined by Title 17 (Radiologic Health Branch) and Title 22 (Department of Health Services) for the State of California. Collaborates with other members of the healthcare team to promote optimum imaging procedures.
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Primary function includes TEM sample preparation of lamella for imaging of client samples using Dual Beam FIB tools. Solid understanding of electron microscopy, semiconductor device physics and failure analysis (through previous work experience or course work.
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Job Description & Requirements Specialty: Mammography Technologist Discipline: Allied Health Professional Duration: Ongoing 40 hours per week Shift: 8 hours, evenings Employment Type: Staff Job Summary: Under the direction of the Imaging Services Director and Chief of Diagnostic Imaging, performs radiographic diagnostic imaging procedures to assist physicians in the diagnosis of disease and injuries.
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This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, CA location in the Abbott Vascular Division. As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Knowledge of mechanical/thermal design (cooling devices, air flow, temperature, power, cooling, mechanical design) with electrical/power (power distribution, AC power types, power calculations, DC power, regulatory/safety) is a plus.
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This role will partner with Clinical Affairs, Medical Affairs, Regulatory, Business Development, Product Development and other cross-functional teams to establish and execute short- and long-term GAVE strategic plans.
$261,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$2,362 a weekFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Minimum of 5 years of experience as a Developer/Business Systems Analyst with a focus on QMS in the medical device industry, including expertise in Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
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Job Responsibilities: Drive the probe-specific optimization of database imaging parameters (55%) Applies his/her specialized skills in acoustics, or related field such as optics, radar, etc., to develop and optimize ultrasound transducers for various imaging modes such as B-mode, CD-mode, etc., on premium medical imaging systems for application on the human body in a clinical environment.
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regulatory affairs molecular imaging jobs Title: sr regulatory specialist in Santa Clara, CA
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