Regulatory affairs Jobs in New Orleans, LA
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Regulatory affairs • new orleans la
Last updated: 4 hours ago
A company is looking for a Regulatory Affairs / Quality Assurance Associate / Specialist.Key Responsibilities : Support the execution and documentation of Corrective and Preventive Actions (CAPAs) ...Show moreLast updated: 30+ days ago
The Tulane Human Research Protection Office (HRPO) administers the University's Human Research Protection Program (HRPP) and Institutional Review Boards (IRBs), which are charged with reviewing and...Show moreLast updated: 30+ days ago
Our Krakenites are a world-class team with crypto conviction, united by our desire to discover and unlock the potential of crypto and blockchain technology.
Kraken is a mission-focused company roote...Show moreLast updated: 11 days ago
Posting Summary Functional Position Title ASSISTANT / ASSOCIATE DEAN OF CLINICAL AFFAIRS Position Number Appointment Type Regular Location-City New Orleans School / Division LSUNO DENTISTRY Departmen...Show moreLast updated: 30+ days ago
Make a Difference in Veteran Care While Enjoying the Vibrant Life in Louisiana!.The Southeast Louisiana VA Health Care Network is dedicated to advocating for a whole health system of care in each o...Show moreLast updated: 24 days ago
Libryo, an ERM Group Company, is a compliance platform that helps global organisations understand and manage their Environmental, Health, and Safety regulatory obligations.Since 2016, Libryo has su...Show moreLast updated: 30+ days ago
At Gilead, we're creating a healthier world for all people.For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapie...Show moreLast updated: 4 hours ago
Summary Information Request Type : PBB / OTL-US Geography : United States Labor Category : PBB (US) Procurement Type : Contingent Labor Organization Unit - Combination of your PID (Process id).Show moreLast updated: 11 days ago
Oversees Graduate Medical Education staff to achieve seamless management and execution of residency and fellowship programs.
Provides oversight and monitors new ACGME-accredited program development ...Show moreLast updated: 30+ days ago
Regulatory Filings Analyst I - Sr.This position will be filled as an Analyst I II III or Sr.This position can be filled in New Orleans LA • •.
The Regulatory Analystcompiles analyzes and provides supp...Show moreLast updated: 2 days ago
Under the general supervision of the Dean of the School of Dentistry this position requires the incumbent to perform highly responsible administrative duties at the level of an Asst / Assoc Dean.This...Show moreLast updated: 10 days ago
Precision Medicine - Medical Affairs Director - Health Systems Oncology.The Precision Medicine - Medical Affairs Director - Health Systems Oncology (PM MAD-HSO) develops ongoing professional relati...Show moreLast updated: 11 days ago
Cargill’s size and scale allows us to make a positive impact in the world.Our purpose is to nourish the world in a safe, responsible and sustainable way.
We are a family company providing food, ingr...Show moreLast updated: 3 days ago
Regulatory Content Manager ERM Libryo – Nashville, TN About ERM Libryo Libryo, an ERM Group Company, is a compliance platform that helps global organisations understand and manage their Environm...Show moreLast updated: 14 days ago
Work Place Flexibility : Hybrid.Legal Entity : Entergy Services, LLC.This position will be filled as an Analyst I - III depending on experience in accordance with relevant qualifications.This positio...Show moreLast updated: 7 days ago
Precision for Medicine is not your typical CRO.At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost...Show moreLast updated: 10 days ago
Ochsner Healthcare Compliance Specialist.We've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate.W...Show moreLast updated: 30+ days ago
Camelback’s flagship program is the Camelback Fellowship.Since 2015, Camelback has raised over $50M and supported 200+ social entrepreneurs – 95% identified as people of color and 60% as women.Our ...Show moreLast updated: 13 days ago
Principal / Sr Medical Writer (Regulatory & Publications).Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We translate unique...Show moreLast updated: 16 days ago
Regulatory Affairs Specialist
VirtualVocationsNew Orleans, Louisiana, United StatesFull-time
Regulatory Compliance Specialist
Tulane UniversityNew Orleans, LA, USFull-time
- Promoted
Senior Product Manager - Margin - Regulatory
KrakenNew Orleans, LA, USFull-time
ASSISTANT / ASSOCIATE DEAN OF CLINICAL AFFAIRS
LSU Health Sciences CenterNew OrleansFull-time
- Promoted
Diagnostic Radiologist
Department of Veterans AffairsNew Orleans, USFull-time
Regulatory Content Manager
ERMNew Orleans, LouisianaFull-time
- Promoted
- New!
ntern Public Affairs, Digital Strategy and Governance
GileadNew Orleans, LA, USFull-time
- Promoted
Senior Manager, Regulatory Information Management!
Abacus Service CorporationNew Orleans, LA, USFull-time
Manager, Academic Affairs - Operations
SHSO-Sutter Health System Office-BayMultiple LocationsFull-time
Regulatory Filings Analyst I Sr.
EntergyNew Orleans, Louisiana, USAFull-time
AsstAssoc Dean Admissions & Student Affairs
Louisiana State University Health Sciences Center PortalNew Orleans, Louisiana, USAFull-time
- Promoted
Precision Medicine - Medical Affairs Director - Health Systems Oncology
MerckNew Orleans, LA, USFull-time
Advisor, FSQR Regulatory Affairs EMEA Cocoa & chocolate.
CargillMultiple LocationsFull-time
ERM Libryo is hiring : Regulatory Content Manager in New Orleans
ERM LibryoNew Orleans, LA, United StatesFull-time
- Promoted
Regulatory Filings Analyst I, II, or III
Louisiana StaffingNew Orleans, LA, USFull-time
- Promoted
Director, Regulatory
Precision for MedicineNew Orleans, LA, USFull-time
- Promoted
Regulatory Licensing Specialist
Ochsner HealthNew Orleans, LA, USFull-time
Chief External Affairs Officer
Camelback VenturesNew Orleans, LA, USFull-time
- Promoted
Principal / Sr Medical Writer (Regulatory & Publications)
Syneos Health / inVentiv Health Commercial LLCNew Orleans, LA, United StatesFull-time
- physician (from $ 59,949 to $ 242,814 year)
- owner operator (from $ 60,000 to $ 240,000 year)
- director of software engineering (from $ 185,000 to $ 239,875 year)
- freelance writing (from $ 38,002 to $ 232,781 year)
- crna (from $ 50,000 to $ 228,000 year)
- independent contractor (from $ 48,750 to $ 225,000 year)
- associate dentist (from $ 50,000 to $ 225,000 year)
- chief financial officer (from $ 125,000 to $ 225,000 year)
- general counsel (from $ 125,842 to $ 222,103 year)
- principal software engineer (from $ 144,814 to $ 222,072 year)
- Boston, MA (from $ 125,771 to $ 200,600 year)
- Cambridge, MA (from $ 113,100 to $ 200,200 year)
- Atlanta, GA (from $ 87,750 to $ 195,950 year)
- San Francisco, CA (from $ 103,208 to $ 195,773 year)
- San Jose, CA (from $ 104,003 to $ 194,780 year)
- San Diego, CA (from $ 104,546 to $ 193,259 year)
- New York, NY (from $ 90,142 to $ 189,903 year)
- Seattle, WA (from $ 95,000 to $ 185,000 year)
- Pittsburgh, PA (from $ 49,920 to $ 177,310 year)
- Houston, TX (from $ 69,257 to $ 170,000 year)
The average salary range is between $ 74,006 and $ 170,765 year , with the average salary hovering around $ 105,135 year .
Regulatory Affairs Specialist
VirtualVocationsNew Orleans, Louisiana, United States30+ days ago
Job type
- Full-time
Job description
A company is looking for a Regulatory Affairs / Quality Assurance Associate / Specialist.
Key Responsibilities :
Support the execution and documentation of Corrective and Preventive Actions (CAPAs)
Assist in vendor qualification, monitoring, and management activities
Maintain and update quality and regulatory documentation (procedures, work instructions, forms, etc.)
Qualifications :
Bachelor's degree in a scientific, engineering, or healthcare-related field OR equivalent experience in regulatory or quality roles within the medical device industry
1-3 years of experience in RA / QA for medical devices (SaMD experience is a plus but not required)
Familiarity with ISO 13485, FDA 21 CFR Part 820, and other relevant regulatory frameworks
Proficiency with document control systems and Microsoft Office tools