Keyword: Molecular Geneticist, Biotech
Job Responsibilities and Requirements: Responsibilities: Develop DNA and RNA molecular assays usCompanya variety of methodologies, including: PCR, DNA sequencing, and fragment analysis. AnalyzCompanyand interpretCompanytest results and complex data. CreatCompanyand writCompanyreports for pathologists and clinicians. LiaisCompanyand collaboratCompanywith colleagues and clinicians. SupportCompanyresearch activities. Responsible for maintainCompanyCAP, CLIA, and ...
This candidate really needs to be a PMP focus with a background in either scientific or healthcare fields. A Master’s or Bachelor’s in a science base field preferred with direction in their career as a PMP.
The Director, Project Management is responsible for working to ensure the overall direction, coordination, execution, monitoring and control, and completion of molecular diagnostic projects within the Caris organization. Work closely with R&D, Operations, Marketing, IT, and Sales ...
Below is a template job description. Every clients job description is a little different.
License/Certification/Education: Normally a B.A./B.S. in Biology and meet all licensing requirements w/1-3 years of experience.
Performs laboratory tests and analyses according to established procedures in designated technical department. Evaluates procedures and methods under direct supervision of more senior technologist, department supervisor, or group leader. Assists in ...
Oversee and manage the daily operations of a scientific team designing, developing, and optimizing, molecular assays for an automated IVD platform.
Candidate must possess prior experience in product development under the design control regulations
Requires a MS or PhD with hands on experience developing assays targeting DNA or RNA including; probe and primer design, nucleic acid hybridization, multiplex PCR, RT PCR, and manufacturing scale up.
Amazing career opportunity to grow within a top ...
MICROBIOLOGIST NEEDED ASAP!!!!!
Identify, isolate and study microorganisms and their byproducts as it relates to the manufacturing and sterilization of medical devices. Work with ethylene oxide and gamma irradiation sterilization techniques. Review biocompatibility tests and interpret the associated industry guidelines. Work with operations and research groups to support continuous quality improvement initiatives.
DUTIES & RESPONSIBILITIES:
-Apply cGLP, cGMP, ANSI, AAMI, ISO, FDA, EPA, and USP ...
Mar 27 -
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