Orthopedic Surgeon
Tunnell Government Services, Inc. · Silver Spring, MD · 1 mo ago
RemoteRemoteHealthcareFull-time
We need to output HTML fragment with sections: headings for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title as heading. Must not include Job ID etc. Remove boilerplate, EEO, etc. Must preserve all substantive info.
Let's parse the posting.
Content:
- Intro about Tunnell Government Services, Inc. (description). Could be "About the role" or maybe "About the company". The instruction says use headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. So we can use "About the role" for description of role and company.
- Mission of FDA CDRH: description.
- Tunnell providing services: description of tasks.
- "Tunnell is seeking a candidate to provide expert consulting services...": description of role.
- Then "Requirements And Qualifications": list of requirements.
We need to split into sections: maybe "About the role" (intro + mission + tasks), "Responsibilities" (list of duties), "Requirements" (maybe combine with qualifications), "Qualifications" (maybe separate). But we should avoid duplication. The posting includes "Requirements And Qualifications" heading with bullet-like list (though not bullet). We can treat that as Requirements and Qualifications combined, or separate.
We need to use
for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title as heading. Must not include Job ID etc. Remove boilerplate, EEO, etc. Must preserve all substantive info.
Let's parse the posting.
Content:
- Intro about Tunnell Government Services, Inc. (description). Could be "About the role" or maybe "About the company". The instruction says use headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. So we can use "About the role" for description of role and company.
- Mission of FDA CDRH: description.
- Tunnell providing services: description of tasks.
- "Tunnell is seeking a candidate to provide expert consulting services...": description of role.
- Then "Requirements And Qualifications": list of requirements.
We need to split into sections: maybe "About the role" (intro + mission + tasks), "Responsibilities" (list of duties), "Requirements" (maybe combine with qualifications), "Qualifications" (maybe separate). But we should avoid duplication. The posting includes "Requirements And Qualifications" heading with bullet-like list (though not bullet). We can treat that as Requirements and Qualifications combined, or separate.
We need to use - for any list of duties/requirements/benefits. So we need to extract list items.
Let's extract duties/responsibilities:
From text: "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."
Also: "Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities."
Thus responsibilities: provide consultation related to supporting medical device reviews; participate in meetings and teleconferences; coordinate meetings; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; execute other administrative office tasks.
We can list those.
Requirements/Qualifications:
- Doctor of Medicine (M.D. or equivalent) from accredited US medical school.
- Current, active, full, unrestricted medical license or registration as a Physician to practice medicine in a State, DC, Puerto Rico, or US territory.
- At least fifteen (10) years of relevant clinical experience (note weird: "At least fifteen (10) years" maybe typo; we keep as written.)
- Certification from a U.S. relevant specialty board organization, e.g., 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 (list examples): 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.
We could treat telework and citizenship as maybe under "Schedule" or "Benefits"? But schedule: "This position is 100% telework." That's schedule info (remote). So we can create a Schedule section with that.
Benefits: Not mentioned. Pay: Not mentioned. So we omit those sections.
We also have some EEO statement etc which we must remove.
Also there is a line: "Tunnell strives to hire and retain the most qualified talent..." that's EEO-ish, remove.
Also "Please be advised that certain client contracts may outline specific requirements for onsite work..." that's maybe a note but could be considered as part of responsibilities? It's about compliance. Might be considered as a note but not boilerplate? It's somewhat generic but still specific to client contracts. Might keep as a responsibility? It says employees expected to comply with all client requirements, including safety and health protocols. Could be a responsibility: comply with client requirements, safety and health protocols. We'll include as a responsibility bullet.
Now structure:
About the role
... intro about Tunnell, mission of FDA CDRH, description of services.
We need to preserve all substantive info; not invent.
Let's craft About the role paragraph:
"Tunnell Government Services, Inc. comprises leading scientists, medical and technical experts, and human capital and organizational development professionals. The company approaches projects as a team and is committed to helping clients transform and quickly achieve strategic goals. The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote public health, ensuring patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. Tunnell provides professional and scientific services to CDRH with expert consultants possessing scientific expertise in the regulation and approval of medical devices."
That seems good.
Now Responsibilities section Responsibilities
with - items.
List items:
- 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
- Execute other administrative office tasks related to CDRH’s projects
- Comply with client requirements, including any safety and health protocols (as per client contracts)
Now Requirements section
Requirements
with list.
But we also have Qualifications; maybe combine into Requirements. However we could split: Requirements (mandatory) and Qualifications (preferred). The posting lumps them together but we can separate: Requirements: MD, license, years experience, board certification, telework/citizenship? Actually telework/citizenship are conditions. Qualifications: thorough understanding, expert in devices, familiarity with FDA processes preferred, communication skills, interpersonal skills.
Let's do:
Requirements
- Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- 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)
- Must be a US Citizen or a Full Green Card holder
- This position is 100% telework
Qualifications
- 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 [bone cutting tools, preparation tools, soft tissue tools]; enabling and smart technologies [robotic-assisted platforms, smart implants, AR/VR guidance, 3‑D custom implants]; external fixation), including specific knowledge of non‑invasive devices 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
We should not include Benefits, Pay, Schedule unless present. Schedule we have as part of Requirements (telework). But we could also make a Schedule section: "This position is 100% telework." However the instruction says only include section when posting has real specific content. It does have schedule info (telework). Could be separate Schedule section. But we already placed it under Requirements. Might be better to have Schedule section. However we must not create thin sections; but schedule is specific. Let's decide: create Schedule section with that line. Then we can remove telework from Requirements.
Thus:
Schedule
This position is 100% telework.
Now Requirements list excludes telework and citizenship? Citizenship is a requirement; keep.
Now we need to ensure we didn't miss any substantive info: The line about "Tunnell strives to hire and retain the most qualified talent..." is EEO, remove. The line about "All qualified applicants will receive consideration for employment without regard to..." is EEO, remove. The line about "Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols." We included as responsibility bullet about complying with client requirements, safety and health protocols. Good.
Now ensure we didn't include any boilerplate like "click on the links below", "contact us", etc. Remove.
Now output only HTML fragment.
Let's craft final HTML:
About the role
Tunnell Government Services, Inc. comprises leading scientists, medical and technical experts, and human capital and organizational development professionals. The company approaches projects as a team and is committed to helping clients transform and quickly achieve strategic goals. The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote public health, ensuring patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. Tunnell provides professional and scientific services to CDRH with expert consultants possessing scientific expertise in the regulation and approval of medical devices.
Responsibilities
- 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
- Execute other administrative office tasks related to CDRH’s projects
- Comply with client requirements, including any safety and health protocols
Requirements
- Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- 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
About the role
... intro about Tunnell, mission of FDA CDRH, description of services.
We need to preserve all substantive info; not invent. Let's craft About the role paragraph: "Tunnell Government Services, Inc. comprises leading scientists, medical and technical experts, and human capital and organizational development professionals. The company approaches projects as a team and is committed to helping clients transform and quickly achieve strategic goals. The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote public health, ensuring patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. Tunnell provides professional and scientific services to CDRH with expert consultants possessing scientific expertise in the regulation and approval of medical devices." That seems good. Now Responsibilities sectionResponsibilities
with- items.
List items:
- 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
- Execute other administrative office tasks related to CDRH’s projects
- Comply with client requirements, including any safety and health protocols (as per client contracts)
Now Requirements section
Requirements
with list. But we also have Qualifications; maybe combine into Requirements. However we could split: Requirements (mandatory) and Qualifications (preferred). The posting lumps them together but we can separate: Requirements: MD, license, years experience, board certification, telework/citizenship? Actually telework/citizenship are conditions. Qualifications: thorough understanding, expert in devices, familiarity with FDA processes preferred, communication skills, interpersonal skills. Let's do:Requirements
- Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- 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)
- Must be a US Citizen or a Full Green Card holder
- This position is 100% telework
Qualifications
- 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 [bone cutting tools, preparation tools, soft tissue tools]; enabling and smart technologies [robotic-assisted platforms, smart implants, AR/VR guidance, 3‑D custom implants]; external fixation), including specific knowledge of non‑invasive devices 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
Schedule
This position is 100% telework.
Now Requirements list excludes telework and citizenship? Citizenship is a requirement; keep. Now we need to ensure we didn't miss any substantive info: The line about "Tunnell strives to hire and retain the most qualified talent..." is EEO, remove. The line about "All qualified applicants will receive consideration for employment without regard to..." is EEO, remove. The line about "Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols." We included as responsibility bullet about complying with client requirements, safety and health protocols. Good. Now ensure we didn't include any boilerplate like "click on the links below", "contact us", etc. Remove. Now output only HTML fragment. Let's craft final HTML:About the role
Tunnell Government Services, Inc. comprises leading scientists, medical and technical experts, and human capital and organizational development professionals. The company approaches projects as a team and is committed to helping clients transform and quickly achieve strategic goals. The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote public health, ensuring patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products. Tunnell provides professional and scientific services to CDRH with expert consultants possessing scientific expertise in the regulation and approval of medical devices.
Responsibilities
- 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
- Execute other administrative office tasks related to CDRH’s projects
- Comply with client requirements, including any safety and health protocols
Requirements
- Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States
- 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