Conduct outreach and health promotion activities in accordance with FDA clinic guidance. * Assist with opening, relocating, or closing occupational health clinic sites as directed. * Respond timely ...
Conduct outreach and health promotion activities in accordance with FDA clinic guidance. * Assist with opening, relocating, or closing occupational health clinic sites as directed. * Respond timely ...
Senior Director, US Regional Regulatory Lead
Boston, MA · On-site
$232K - $284K/yr
Knowledgeable in ICH, FDA guidelines and requirements * Well organized, scientifically driven, detailed oriented, pragmatic * Open minded, respectful and excels at teamwork * Self-directed, solution ...
Senior Director, US Regional Regulatory Lead
Boston, MA · On-site
$232K - $284K/yr
Knowledgeable in ICH, FDA guidelines and requirements * Well organized, scientifically driven, detailed oriented, pragmatic * Open minded, respectful and excels at teamwork * Self-directed, solution ...
S. regulatory submissions to the FDA for investigational and commercial products. The position ... open to learning and adapting in a fast-paced, deadline-driven environment. This role requires ...
S. regulatory submissions to the FDA for investigational and commercial products. The position ... open to learning and adapting in a fast-paced, deadline-driven environment. This role requires ...
Quality Supervisor
$60K - $72K/yr
... FDA, GMP, Continuous Improvement** Company Description Libertyjobs.com has become an essential destination site for experienced job seekers. Our recruiters are continually posting active job openings ...
Quick apply
Quality Supervisor
$60K - $72K/yr
... FDA, GMP, Continuous Improvement** Company Description Libertyjobs.com has become an essential destination site for experienced job seekers. Our recruiters are continually posting active job openings ...
Support FDA submissions including 510(k), Technical Files, and other regulatory filings as required ... If you are open to exploring new roles or would like to stay informed about relevant positions ...
Quick apply
Support FDA submissions including 510(k), Technical Files, and other regulatory filings as required ... If you are open to exploring new roles or would like to stay informed about relevant positions ...
Porter
$10/hr
Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Experience with FDA, GMP regulated industries a plus. Additional Information All your information ...
Porter
$10/hr
Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Experience with FDA, GMP regulated industries a plus. Additional Information All your information ...
Our industry-leading intraoral scanners and open-platform software are transforming dental ... S., Canada, and LATAM -- including FDA Class II 510(k) submissions, ISO 13485 quality systems, and ...
Quick apply
Our industry-leading intraoral scanners and open-platform software are transforming dental ... S., Canada, and LATAM -- including FDA Class II 510(k) submissions, ISO 13485 quality systems, and ...
Visit us at -a-job/ to learn more and view our open positions. Please apply or call one of us to ... Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR ...
Quick apply
Visit us at -a-job/ to learn more and view our open positions. Please apply or call one of us to ... Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR ...
Records Management Specialist I (General Clerk)
College Park, MD · On-site
$18/hr
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
Records Management Specialist I (General Clerk)
College Park, MD · On-site
$18/hr
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
EP Cardiology Opening in Wausau, WI
Wausau, WI · On-site
$379K - $428K/yr
EP Cardiology opening in Wisconsin - Located in Wausau, WI - Green Bay 100m - Full-time, permanent ... for FDA DEEP trial using a combined EP and surgical approach to persistent and long standing ...
EP Cardiology Opening in Wausau, WI
Wausau, WI · On-site
$379K - $428K/yr
EP Cardiology opening in Wisconsin - Located in Wausau, WI - Green Bay 100m - Full-time, permanent ... for FDA DEEP trial using a combined EP and surgical approach to persistent and long standing ...
Records Management Specialist I (General Clerk)
College Park, MD · On-site
$18/hr
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
Quick apply
Records Management Specialist I (General Clerk)
College Park, MD · On-site
$18/hr
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to ... Lead FDA interactions including in-person meetings, teleconferences, written submissions and other ...
DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to ... Lead FDA interactions including in-person meetings, teleconferences, written submissions and other ...
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews ... Open, process, and distribute incoming mail; create and affix barcode labels * Retrieve documents ...
DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to ... Lead FDA interactions including in-person meetings, teleconferences, written submissions and other ...
Quick apply
DEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to ... Lead FDA interactions including in-person meetings, teleconferences, written submissions and other ...
Senior Quality Engineer
Chicago, IL · On-site +1
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Senior Quality Engineer
Chicago, IL · On-site +1
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Quality Control Analyst I
$23.50 - $31.75/hr
We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA's ChemStewards ® Management ... Experience with Open Lab, Chem Station and/or Empower analytical software preferred. * Proficiency ...
Quality Control Analyst I
$23.50 - $31.75/hr
We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA's ChemStewards ® Management ... Experience with Open Lab, Chem Station and/or Empower analytical software preferred. * Proficiency ...
Senior Regulatory Affairs Specialist (Columbia, MD)
Columbia, MD · Hybrid
$101K - $152K/yr
Participate and support FDA audits/inspections to maintain all necessary certifications/approvals ... We anticipate the application window for this opening to close on 08.07.2026 **This position does ...
Senior Regulatory Affairs Specialist (Columbia, MD)
Columbia, MD · Hybrid
$101K - $152K/yr
Participate and support FDA audits/inspections to maintain all necessary certifications/approvals ... We anticipate the application window for this opening to close on 08.07.2026 **This position does ...
Quality Inspector
$12 - $15/hr
Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Requirements: 1 - 2 years' experience in related field Knowledge of FDA/cGMP guidelines Basic ...
Quality Inspector
$12 - $15/hr
Company Description Open Scientific provides contract staffing and direct hire recruitment services ... Requirements: 1 - 2 years' experience in related field Knowledge of FDA/cGMP guidelines Basic ...
Senior Quality Engineer
Chicago, IL · On-site
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Senior Quality Engineer
Chicago, IL · On-site
Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...
Fda Openings information
What are the key skills and qualifications needed to thrive in FDA job openings, and why are they important?
What are some common challenges faced by professionals starting in FDA roles, and how can applicants prepare for them?
What are FDA openings?
- Entry Level Regulatory Affairs Biotech
- Entry Level Regulatory Affairs Cosmetics
- Samd Regulatory
- Regulatory Affairs Junior
- Regulatory Affairs
- Executive Biotech Regulatory Affairs
- Regulatory Affairs Associate
- Locum Pharmaceutical Regulatory Affairs
- Internship Biotech Regulatory Affairs
- Freelance Biotech Regulatory Affairs

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 2 days ago
Job description
ServeFed is seeking a Full-Time Registered Nurse in support of the Food and Drug Administration (FDA) Occupational Health Clinic in Laurel, MD.
Seize the Opportunity!
At ServeFed, we’re committed to connecting exceptional healthcare professionals with our federal clients. We hire individuals who bring passion, innovation, and expertise to their work across healthcare, IT, accounting, finance, health and safety, and workforce management. Join our talent community and build a rewarding career supporting a mission-driven federal agency.
- Excellent Compensation amp; Comprehensive Benefits
- Paid Vacation, Paid Sick
- 11 Paid Federal Holidays
- Medical/Dental/Vision Benefits
- Company Paid Short-Term Disability, Long-Term Disability, Accidental Death amp; Dismemberment amp; Life Insurance
- 401(k)
- Health and Welfare Benefit
- No nights
- No weekend responsibility
- Provide healthcare services directly to FDA employees and authorized clients at assigned occupational health clinic (OHC) locations in accordance with state scope of practice, FDA clinic policies, and standard operating procedures (SOPs).
- Perform components of physical examinations, including:
- Vital signs, height, and weight
- Audiometry
- Vision testing
- ECG
- Spirometry
- Phlebotomy
- TB skin testing
- Accurately document all clinical data on required forms and in designated systems.
- Administer immunizations in accordance with FDA clinic policies, SOPs, and standing orders.
- Provide non-emergency clinical care to FDA clients per Registered Nurse protocols.
- Respond to medical emergencies and provide care in accordance with BLS/AED protocols and FDA clinic procedures.
- Administer medications as ordered by authorized external prescribing physicians, when approvals are current and on file.
- Provide and review destination-specific travel health information for FDA employees.
- Perform respirator fit testing, as required at assigned sites.
- Conduct outreach and health promotion activities in accordance with FDA clinic guidance.
- Assist with opening, relocating, or closing occupational health clinic sites as directed.
- Respond timely and accurately to data and reporting requests from clinic leadership and medical oversight officials.
- Maintain competency in all site-specific clinical tasks required to support FDA occupational health services.
• Licensed: As a Registered Nurse (RN) in the state where the nurse practices.
• Experience: At least (3) years of post-graduate clinical experience as a RN providing direct patient care. At least (3) years clinical experience in Occupational Health, Preventive Medicine or Public Health experience is preferred and will be considered a strength.
• Biannual certification in BLS for Healthcare Providers.