Entry Writer
$25 - $28/hr
W, etc.) including FDA Prior Notice * Maintain customer confidentiality where applicable Key Requirements:
$25 - $28/hr
W, etc.) including FDA Prior Notice * Maintain customer confidentiality where applicable Key Requirements:
$25 - $28/hr
W, etc.) including FDA Prior Notice * Maintain customer confidentiality where applicable Key Requirements:
Clackamas, OR · On-site
This role focuses on reviewing and releasing raw materials and finished products, supporting production, and ensuring compliance with FDA/cGMP standards. Key Responsibilities * Review, approve, and ...
Clackamas, OR · On-site
This role focuses on reviewing and releasing raw materials and finished products, supporting production, and ensuring compliance with FDA/cGMP standards. Key Responsibilities * Review, approve, and ...
Portland, OR · On-site
$25 - $28/hr
File Partner Government Agency (PGA) data sets (FDA, F&W, etc.) including FDA Prior Notice * Maintain customer confidentiality where applicable Key Requirements: * 2+ years relevant Freight ...
Portland, OR · On-site
$25 - $28/hr
File Partner Government Agency (PGA) data sets (FDA, F&W, etc.) including FDA Prior Notice * Maintain customer confidentiality where applicable Key Requirements: * 2+ years relevant Freight ...
Portland, OR · On-site
Experience working in an FDA regulated industry/field or similar * Exposure to the FDA 510(k) process or other regulatory submissions preferred. * Experience in a LEAN Manufacturing/Production ...
Quick apply
Portland, OR · On-site
Experience working in an FDA regulated industry/field or similar * Exposure to the FDA 510(k) process or other regulatory submissions preferred. * Experience in a LEAN Manufacturing/Production ...
Portland, OR · On-site
Experience working in an FDA regulated industry/field or similar * Exposure to the FDA 510(k) process or other regulatory submissions preferred. * Experience in a LEAN Manufacturing/Production ...
Quick apply
Portland, OR · On-site
Experience working in an FDA regulated industry/field or similar * Exposure to the FDA 510(k) process or other regulatory submissions preferred. * Experience in a LEAN Manufacturing/Production ...
Portland, OR · On-site
Capable to understand the code of JDE Applications using FDA (Form Design Aid), RDA (Report Design Aid), and TDA (Table Design Aid) * Troubleshoot and resolve technical issues related to JDE objects ...
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Portland, OR · On-site
Capable to understand the code of JDE Applications using FDA (Form Design Aid), RDA (Report Design Aid), and TDA (Table Design Aid) * Troubleshoot and resolve technical issues related to JDE objects ...
ESSENTIAL FUNCTIONS) 1. Perform mammographic examinations as required by MQSA/FDA guidelines and by departmental protocols* 2. Perform weekly and Monthly QC monitoring, charting and documenting of ...
ESSENTIAL FUNCTIONS) 1. Perform mammographic examinations as required by MQSA/FDA guidelines and by departmental protocols* 2. Perform weekly and Monthly QC monitoring, charting and documenting of ...
Hillsboro, OR · On-site
$78K - $101K/yr
This role drives quality objectives during product development, ensuring compliance with FDA, ISO 13485, and other global standards. The QE II serves as the Quality lead during development and ...
Hillsboro, OR · On-site
$78K - $101K/yr
This role drives quality objectives during product development, ensuring compliance with FDA, ISO 13485, and other global standards. The QE II serves as the Quality lead during development and ...
Hillsboro, OR · On-site
$78K - $101K/yr
This role drives quality objectives during product development, ensuring compliance with FDA, ISO 13485, and other global standards. The QE II serves as the Quality lead during development and ...
Hillsboro, OR · On-site
$78K - $101K/yr
This role drives quality objectives during product development, ensuring compliance with FDA, ISO 13485, and other global standards. The QE II serves as the Quality lead during development and ...
Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations. Defect Management: Identifies, classifies ...
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Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations. Defect Management: Identifies, classifies ...
Portland, OR · On-site
Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations. Defect Management: Identifies, classifies ...
Quick apply
Portland, OR · On-site
Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations. Defect Management: Identifies, classifies ...
$25.75 - $34.25/hr
The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced ...
$25.75 - $34.25/hr
The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced ...
Troutdale, OR · On-site
$70K - $78K/yr
Instrumental in the incorporation and solidification of food security requirements per FDA and customer guidelines * Assist the Corporate Food Safety Department and company facilities in developing ...
Troutdale, OR · On-site
$70K - $78K/yr
Instrumental in the incorporation and solidification of food security requirements per FDA and customer guidelines * Assist the Corporate Food Safety Department and company facilities in developing ...
Troutdale, OR · On-site
$70K - $78K/yr
Instrumental in the incorporation and solidification of food security requirements per FDA and customer guidelines * Assist the Corporate Food Safety Department and company facilities in developing ...
Troutdale, OR · On-site
$70K - $78K/yr
Instrumental in the incorporation and solidification of food security requirements per FDA and customer guidelines * Assist the Corporate Food Safety Department and company facilities in developing ...
Portland, OR · On-site
$17.56 - $26.67/hr
The Opportunity As our Food Quality Specialist, you will play a key role in ensuring compliance with all major food safety and regulatory standards including FDA, USDA, HACCP, and our company ...
Portland, OR · On-site
$17.56 - $26.67/hr
The Opportunity As our Food Quality Specialist, you will play a key role in ensuring compliance with all major food safety and regulatory standards including FDA, USDA, HACCP, and our company ...
Portland, OR · On-site
$18 - $22/hr
Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...
Portland, OR · On-site
$18 - $22/hr
Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...
$18 - $22/hr
Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...
$18 - $22/hr
Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...
Portland, OR · On-site
$25.75 - $34.25/hr
The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced ...
Portland, OR · On-site
$25.75 - $34.25/hr
The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced ...
Portland, OR · On-site
$17.75 - $21.50/hr
Food and Drug Administration (FDA) regulations, other regulatory requirements.
Portland, OR · On-site
$17.75 - $21.50/hr
Food and Drug Administration (FDA) regulations, other regulatory requirements.
Portland, OR · On-site
$17.75 - $21.50/hr
Comply with FDA regulations, company policies, standard operating procedures (SOPs), and other applicable regulatory requirements. * Maintain positive working relationships with employees, customers ...
Portland, OR · On-site
$17.75 - $21.50/hr
Comply with FDA regulations, company policies, standard operating procedures (SOPs), and other applicable regulatory requirements. * Maintain positive working relationships with employees, customers ...
| Aspect | Fda | Food Scientist |
|---|---|---|
| Required Credentials | Typically a degree in health, science, or related field; certifications vary | Bachelor's or master's in food science, microbiology, or related |
| Work Environment | Regulatory agencies, laboratories, inspection sites | Food manufacturing facilities, laboratories, research settings |
| Employer & Industry Usage | U.S. Food and Drug Administration, government agencies | Food companies, research institutions, government agencies |
| Common Search & Comparison Intent | Understanding regulatory roles, compliance, and enforcement | Food safety, product development, research |
While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

$25 - $28/hr
Full-time
Posted 12 days ago
Customs Entry Writer
Janel Group is seeking a Customs Entry Writer to join our team! If you’re a high-energy, focused freight forwarding professional who wants to continue building your customs brokerage and freight-forwarding career with a customer-focused, fast-paced industry leader, we'd love to talk!
Primary Responsibilities:
Preparing and filing Customs entry documentation in compliance with US Customs regulations
Proactively and aggressively resolve logistics and transportation issues with a customer-centered focus
Collaborating with the team to deliver outstanding service to our customers while leveraging opportunities to grow our business
Data entry of client shipment detail and update of shipment milestones
Create and monitor exception reports in a consistent and timely manner
Actively communicate with customers to ensure 100% satisfaction and full visibility of shipment status
File Partner Government Agency (PGA) data sets (FDA, F amp;W, etc.) including FDA Prior Notice
Maintain customer confidentiality where applicable
Key Requirements: