Biomedical Engineer/Medical Device Subject Matter Expert (RK)
Job Description
Biomedical Engineer / Medical Device Subject Matter Expert
to Support Respiratory and Medical Device and Diagnostics Development
Background: The DHHS is responsible for advanced development and procurement of medical countermeasures to public health threats in the form of naturally occurring diseases such as influenza and weaponized chemical, biological, and radiation terrorist actions. They complete this mission through contracting actions to the industry that will develop, gain FDA approval and produce for storage necessary countermeasures.
DHHS must careful describe the need within solicitations and then upon award of contract monitor progress against set cost, schedule, and performance guidelines. These actions require subject matter experts in several different disciplines of medical pharmaceutical and device development and manufacturing.
Within this larger portfolio are respiratory devices that can provide support to respiratory compromised patients during pandemic influenza outbreaks or any all-hazards events. This includes durable re-useable medical devices and respiratory protection devices for use in austere locations and often without direct medical personnel oversight. The DHHS requires a subject matter expert who can provide necessary expertise in the engineering development, regulatory compliance, and clinical usage of such devices.
The subject matter expert may also be assigned to support the development and manufacturing of other medical devices and diagnostics that could be used counter CBRN, influenza and emerging infectious disease threats.
Duties of the position: The DHHS requires an individual with strong biomedical engineering and design skills to assist in the following manner:
•Conduct market surveys of respiratory protection and other medical device/diagnostic technologies against public health emergency response need and understanding the ramifications of technologies to environment, ease of use, and ultimate clinical usage requirements/satisfaction.
•Assist in technology selection from administration through review of technical proposals and providing recommendations to the project management team.
•Assist in the preparation of solicitations for research projects to develop and manufacture respiratory devices, from masks to ventilators, and other medical devices and diagnostics in support of DHHS requirements.
•Understand regulatory implications of technologies and assist the Project Manager and contracted manufacturer in developing a feasible and economical regulatory path with acceptable risk.
•Assist in the development of project plans task to schedule and then monitor progress periodically for compliance.
•Assist in the management of contract to include assessment of contracted device manufacturer progress, technology or schedule risk identifications, and resolution recommendations.
Experience:
•Minimum of 10 (15+ years preferred) years of experience in biomedical equipment/device development and manufacturing
•At least 5 years of experience with development/manufacturing of respiratory devices
•The desired candidate will have: Participated on a development team that took a respiratory device fully through FDA approval (510(k) minimum; IDE preferred).
An understanding of and experience with human factors engineering and testing for medical devices
Interfaced with clinical staff to establish and evaluate design and functional requirements. Experience in development of design characteristics of respiratory devices a definitive plus.
•Excellent written and oral communication skills are necessary.
•Ability to multi-task varying projects and activities to meet deadlines
Education:
•Minimum: Bachelors in Biomedical Engineering
•Preferred: Master’s Degree in Biomedical Engineering
COMPENSATION
Benefits - Full
Relocation Assistance Available - Possible for ideal candidate
CANDIDATE DETAILS
15+ years experience
Management Experience Required - No
Minimum Education - Bachelor's Degree
Willingness to Travel - Occasionally
ADDITIONAL DETAILS
Location: Washington, D.C.
Industry: Pharmaceutical / Biotech
Job Category: Engineering - Other Engineering
Hours Per Week: 4-+
We have remote access to the computer system the company uses. I will be able to place your resume directly into an active candidate queue. In addition we can champion you to top management.
If you have worked at a similar company and held a similar position, this is what I will need from you:
A current copy of your resume with full address sent to me as an attachment. We cannot use the online version. PLEASE MAKE SURE YOUR RESUME HAS YOUR FULL ADDRESS AND CONTACT INFORMATION,
BE SMART- Make sure your resume has all the KEY WORDS from the job description. Resumes without the KEY WORDS are ignored by the HR people.
Your citizenship or visa status.
Your desired base salary range.
Are you willing to relocate if necessary? Will you have to relocate if you get this job?
We are always company paid. We do not accept money from candidates. We are paid by them but we work for you.
Job Description
Biomedical Engineer / Medical Device Subject Matter Expert
to Support Respiratory and Medical Device and Diagnostics Development
Background: The DHHS is responsible for advanced development and procurement of medical countermeasures to public health threats in the form of naturally occurring diseases such as influenza and weaponized chemical, biological, and radiation terrorist actions. They complete this mission through contracting actions to the industry that will develop, gain FDA approval and produce for storage necessary countermeasures.
DHHS must careful describe the need within solicitations and then upon award of contract monitor progress against set cost, schedule, and performance guidelines. These actions require subject matter experts in several different disciplines of medical pharmaceutical and device development and manufacturing.
Within this larger portfolio are respiratory devices that can provide support to respiratory compromised patients during pandemic influenza outbreaks or any all-hazards events. This includes durable re-useable medical devices and respiratory protection devices for use in austere locations and often without direct medical personnel oversight. The DHHS requires a subject matter expert who can provide necessary expertise in the engineering development, regulatory compliance, and clinical usage of such devices.
The subject matter expert may also be assigned to support the development and manufacturing of other medical devices and diagnostics that could be used counter CBRN, influenza and emerging infectious disease threats.
Duties of the position: The DHHS requires an individual with strong biomedical engineering and design skills to assist in the following manner:
•Conduct market surveys of respiratory protection and other medical device/diagnostic technologies against public health emergency response need and understanding the ramifications of technologies to environment, ease of use, and ultimate clinical usage requirements/satisfaction.
•Assist in technology selection from administration through review of technical proposals and providing recommendations to the project management team.
•Assist in the preparation of solicitations for research projects to develop and manufacture respiratory devices, from masks to ventilators, and other medical devices and diagnostics in support of DHHS requirements.
•Understand regulatory implications of technologies and assist the Project Manager and contracted manufacturer in developing a feasible and economical regulatory path with acceptable risk.
•Assist in the development of project plans task to schedule and then monitor progress periodically for compliance.
•Assist in the management of contract to include assessment of contracted device manufacturer progress, technology or schedule risk identifications, and resolution recommendations.
Experience:
•Minimum of 10 (15+ years preferred) years of experience in biomedical equipment/device development and manufacturing
•At least 5 years of experience with development/manufacturing of respiratory devices
•The desired candidate will have: Participated on a development team that took a respiratory device fully through FDA approval (510(k) minimum; IDE preferred).
An understanding of and experience with human factors engineering and testing for medical devices
Interfaced with clinical staff to establish and evaluate design and functional requirements. Experience in development of design characteristics of respiratory devices a definitive plus.
•Excellent written and oral communication skills are necessary.
•Ability to multi-task varying projects and activities to meet deadlines
Education:
•Minimum: Bachelors in Biomedical Engineering
•Preferred: Master’s Degree in Biomedical Engineering
COMPENSATION
Benefits - Full
Relocation Assistance Available - Possible for ideal candidate
CANDIDATE DETAILS
15+ years experience
Management Experience Required - No
Minimum Education - Bachelor's Degree
Willingness to Travel - Occasionally
ADDITIONAL DETAILS
Location: Washington, D.C.
Industry: Pharmaceutical / Biotech
Job Category: Engineering - Other Engineering
Hours Per Week: 4-+
We have remote access to the computer system the company uses. I will be able to place your resume directly into an active candidate queue. In addition we can champion you to top management.
If you have worked at a similar company and held a similar position, this is what I will need from you:
A current copy of your resume with full address sent to me as an attachment. We cannot use the online version. PLEASE MAKE SURE YOUR RESUME HAS YOUR FULL ADDRESS AND CONTACT INFORMATION,
BE SMART- Make sure your resume has all the KEY WORDS from the job description. Resumes without the KEY WORDS are ignored by the HR people.
Your citizenship or visa status.
Your desired base salary range.
Are you willing to relocate if necessary? Will you have to relocate if you get this job?
We are always company paid. We do not accept money from candidates. We are paid by them but we work for you.