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Temp Roche Tissue Diagnostics Jobs in Maryland (NOW HIRING)

Temp Roche Tissue Diagnostics information

What is the difference between Temp Roche Tissue Diagnostics vs Temp Histology Technician?

AspectTemp Roche Tissue DiagnosticsTemp Histology Technician
CertificationsTypically requires histology or pathology certificationsRequires histology or laboratory technician certifications
Work EnvironmentWorks in clinical labs, hospitals, or diagnostic facilitiesWorks in pathology labs, hospitals, or research institutions
Industry UsageUsed in diagnostic imaging and tissue analysisUsed in tissue processing and slide preparation
Job ResponsibilitiesAssists with tissue diagnostics, slide preparation, and stainingPrepares tissue samples, sectioning, and staining

Both roles involve working with tissue samples in diagnostic or laboratory settings, but Temp Roche Tissue Diagnostics focuses more on tissue analysis and diagnostics, while Temp Histology Technician emphasizes tissue processing and slide preparation. They share similar certifications and work environments, making them closely related in the pathology industry.

What are the most commonly searched types of Roche Tissue Diagnostics jobs in Maryland?

The most popular types of Roche Tissue Diagnostics jobs in Maryland are:

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The top searched job categories for Temp Roche Tissue Diagnostics jobs in Maryland are:

What cities in Maryland are hiring for Temp Roche Tissue Diagnostics jobs?

Cities in Maryland with the most Temp Roche Tissue Diagnostics job openings:

Full-time

Re-posted 3 days ago


Job description

Medical Officer (Orthopedic Surgeon) SME Position Description 

The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.

Tunnell Government Services, Inc. is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH's projects.

Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in clinical medicine and orthopedic surgery, as relevant to medical devices.

Requirements and Qualifications

  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • In addition, the candidate must possess a current, active, full, and unrestricted medical license or registration as a Physician to practice medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • At least fifteen (10) years of relevant clinical experience
  • Certification from a U.S. relevant specialty board organization, e.g., the American Board of Orthopedic Surgery (ABOS), etc.
  • Thorough understanding of current clinical practices in orthopedic surgery, including diagnosis and treatment, and current/emerging trends in practice.
  • Expert in function and utilization of medical devices commonly used as part of orthopedic surgery (e.g., permanent and temporary implants [prostheses, fixation devices, osteobiologics], surgical instruments (e.g., bone cutting tools, preparation tools, soft tissue tools), enabling and smart technologies [robotic-assisted platforms, smart implants, AR/VR guidance, 3-D custom implants], and external fixation) to include specific knowledge of non-invasive devices and instruments used for diagnosis; invasive devices, such as implantable devices; and surgical systems.
  • Familiarity with FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 878 - General and Plastic Surgery Devices), and guidances is preferred.
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.

This position is 100% telework. 

Must be a US Citizen or a Full Green Card holder.