34 fda opportunities in Brea updated today
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BaRupOn LLCRegulatory Affairs Specialist (FDA, DEA) The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audit
Staffmark GroupJob Title: Regulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM - 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commitment) Role Overview An established consulting firm in Torra
A leading medical device company located in California, USA, is seeking a driven Project Manager to lead cross-functional teams in the development and commercialization of innovative medical devices. The ideal candidate will have 4-10 years of experience in managing medical device programs with a st
A leading staffing firm is seeking a Digital Lab Email Specialist to manage email marketing programs in a regulated FDA-compliant environment. Responsibilities include building and testing emails, coordinating with stakeholders, and ensuring compliance. Ideal candidates have 3-5 years of email marke
A recruitment agency is seeking a detail-oriented Software Verification Engineer to join an innovative verification team in Los Angeles, CA. The role requires strong coding skills and a Bachelor's degree in relevant fields. The engineer will conduct test planning, execution, and defect resolution in
BaRupOn LLCJob Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv
Staffmark GroupJapanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full-time Work Hours: 09:00 am - 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and bilingual FDA Research Consultant to join their team. This role se
StaffmarkJapanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full-time Work Hours: 09:00 am - 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and bilingual FDA Research Consultant to join their team. This role se
StaffmarkJob Title: Regulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM - 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commitment) Role Overview An established consulting firm in Torra
Innovative Career Resources & StaffingA recognized medical diagnostics manufacturer in Southern California is seeking a Senior Quality Control Inspector to ensure regulatory compliance and product quality. The ideal candidate will have over 5 years of experience in FDA-regulated environments, a strong understanding of ISO 13485, and pro
BiVACORA leading medical device manufacturer in Huntington Beach is seeking an experienced Quality Inspector IV to support the development of a world-first Total Artificial Heart. This role involves hands-on inspection in an FDA-regulated environment, requiring strong knowledge of quality standards and tec
National Institute of Clinical Research, Inc.A leading clinical research organization in California is seeking an experienced Quality Assurance Specialist to ensure the accuracy and compliance of clinical research data. This role requires overseeing audits and compliance with FDA regulations while providing training to research staff. Candidat
Japanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full‑time Work Hours: 09:00 am – 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and bilingual FDA Research Consultant to join their team. This role se
Staffmark GroupJob Title: Regulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM - 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commitment) Role Overview An established consulting firm in Torra
Japanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full-time Work Hours: 09:00 am - 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and bilingual FDA Research Consultant to join their team. This role se
StaffmarkRegulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commitment) Role Overview An established consulting firm in Torrance, serving
A consulting firm in Torrance, CA is seeking a Japanese Bilingual FDA Research Consultant to act as a liaison between US regulatory bodies and Japanese clients. Responsibilities include conducting research on US regulations, preparing regulatory documents, and analyzing data to provide consulting re
A leading dental products company in Irvine, California, is seeking a Regulatory Affairs professional to manage product registrations and ensure compliance with FDA and other regulatory bodies. The ideal candidate will have over five years of experience and a Bachelor's degree in a related field. Th
A leading Biotech Consultancy firm is seeking a SAP Computer System Validation (CSV) Analyst to join their remote team. This role involves reviewing and validating SAP test scripts in a GxP-regulated environment. Ideal candidates should have over 3 years of SAP CSV experience, strong knowledge of FD
A leading medical device company seeks a Quality Engineer for Risk Management in Irvine, CA. This role involves developing compliant risk management frameworks for cardiac devices and ensuring adherence to FDA regulations. Candidates should have 8–12 years of experience in Medical Device Quality, fo
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a cu
BaRupOn LLCJob Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolv
### **Job Summary** The **Regulatory Affairs Specialist (FDA, DEA)** will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ah
A leading dietary supplement manufacturer in California is looking for a Production Supervisor to oversee production activities. This position requires 3-5 years of supervisory experience in an FDA environment, alongside strong communication and multitasking skills. The supervisor will ensure that a
Job Title: Regulatory Affairs Specialist (FDA/Medical Device) Location: Torrance, CA Type: Full-time (On-site) Schedule: 9:00 AM - 6:00 PM (Offers flexibility in occasions for your needs to take care of your family members or academic commitment) Role Overview An established consulting firm in Torra
A leading consulting firm in Torrance is seeking a Regulatory Affairs Specialist. The role requires managing regulatory submissions, coordinating with US regulatory bodies, and extensive research on FDA/EPA regulations. Ideal candidates will hold a Bachelor's in a STEM field, show meticulous attenti
Japanese Bilingual FDA Research & Regulatory Consultant Employment Type: Full-time Work Hours: 09:00 am - 6:00 pm (Flexible arrangements available) Work Location: Torrance, CA Job Overview A consulting firm is seeking a dedicated and bilingual FDA Research Consultant to join their team. This role se
A leading food safety company is seeking a Quality Assurance Supervisor to oversee QA functions in a refrigerated prepared foods plant. The ideal candidate will have at least 10 years of experience in QA, particularly in USDA Food safety. This full-time role involves ensuring compliance with both US
A leading firm in Medical Devices is seeking a Senior Quality Engineer in Irvine, California. The successful candidate will establish a compliant risk management framework and lead remediation efforts for existing documentation. Ideal applicants will have over 7 years of experience in Medical Device
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Brea. Actual salaries may vary depending on experience, company, and area.
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