Regulatory Affairs Specialist (FDA, DEA )
BaRupOn LLC
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 ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances. Key Responsibilities Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates) Oversee and renew DEA registrations, inventory records, and security documentation Maintain state pharmacy, medical device, and wholesale distribution licenses Track regulatory changes affecting compounding, controlled substances, and labeling requirements Support internal audits, site inspections, and responses to 483s or warning letters Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports Serve as point of contact with federal and state regulatory agencies Document and file compliance records and ensure timely reporting Qualifications Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor’s preferred) 2–4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements Strong writing, documentation, and organizational skills Familiarity with electronic submission systems, labeling requirements, and drug master files Preferred Skills Experience in sterile or non-sterile compounding (503A or 503B environments) Knowledge of NABP license portals, MedWatch reporting, or REMS programs Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) Experience responding to FDA inspections, audits, or state pharmacy board requests Benefits Health, dental, and vision insurance 401(k) with employer match Paid time off and holidays Regulatory training and continuing education support Advancement opportunities into QA/RA leadership roles #J-18808-Ljbffr
- ...similar. 5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project... ...the IVD industry. Knowledge of FDA, and CE marking requirements for IVD products... ...Thorough knowledge of policies, practices and procedures related to Regulatory Affairs....Suggested
- ...Responsibilities: Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on... ...experience) 6 - 8 years working in a regulated industry (FDA and Software as a Medical Device preferred). Strong knowledge...Suggested
$85k - $130k
Job SummarySr Regulatory Affairs Specialist is an accomplished regulatory professional with a successful work history with leading regulatory initiatives... ...product listings and establishment registrations with FDA.Maintain regulatory databases and summary reports to support...SuggestedWork experience placementLocal areaWorldwideFlexible hours$92k - $148.35k
...and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory... ...talent for a Senior Regulatory Affairs Specialist. This role will work a Hybrid/Flex schedule... ...Experience interacting directly with US FDA required, EU MDR experience preferred.Ability...SuggestedFull timeContract workTemporary workLocal areaImmediate startFlexible hours3 days per week- ...position is responsible for the preparation of regulatory submissions required to market medical... ...registrations and related regulatory affairs activities, including execution of procedures... ...of industry consensus standards and FDA guidance is required At least 2 years Regulatory...SuggestedWork at office
- Regulatory Affairs Specialist II (hybrid) The Regulatory Affairs Specialist III, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs...Full timeWork at officeWorldwideDay shift
$110.1k - $183.4k
Work Flexibility: Hybrid or OnsiteStaff International Regulatory Affairs SpecialistIrvine, CAIn this International Regulatory Affairs role, you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways. This is a meaningful...Full timeFor contractorsLocal area$90k - $140k
...Regulatory Strategy Lead Execute on regulatory strategy of De Novo submissions for AI/ML-based Software as a Medical Device (SaMD) product... ...genomic and proteomic biomarkers. Ensure alignment with FDA expectations for Breakthrough Device Designation (BDD), SaMD, and...- ...submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies. Maintains company registrations and device listings... ...Minimum five (5) years of experience in Regulatory Affairs. Experience in preparing (writing) domestic and international...
- ...Jenavalve Technology is hiring a Senior Specialist for Regulatory Affairs in Irvine, CA with a strong focus on managing regulatory communication and submissions. The role requires substantial experience in medical device regulations, ensuring compliance with quality standards...
- ...cardiovascular and interventional space. As the company continues to expand its global footprint, they are seeking a Senior Regulatory Affairs Specialist to support regulatory strategy, submissions, and global compliance activities across the product lifecycle. This is an...
- ...The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is looking for... .... The Principal Regulatory Affairs Specialist is a senior technical expert and strategic... ...You will lead the execution of key U.S. FDA submissions—including IDEs, 510(k)s,...Full timeContract workRemote work3 days per week
$120k - $155k
...Lead regulatory strategy and submission activities for Qnovia's drug-device combination products across FDA, MHRA, and other global regulatory bodies. About the Role Qnovia is... ...and United Kingdom. As a Regulatory Affairs Specialist, you will develop and execute regulatory...Local areaFlexible hours- ...Regulatory Affairs Specialist Responsibilities Regulatory Affairs is responsible for planning, coordinating and implementing regulatory submissions for products that require government approval. Demonstrates working knowledge of healthcare-related regulations. Demonstrates...Contract work
- ...is a division of Glidewell Dental. We are seeking an experienced Regulatory Affairs Specialist to support global regulatory compliance and drive high‑impact submissions. In this role, you’ll lead FDA 510(k)/PMA filings, maintain international registrations, support audits...
- Immediate hire for a Jr. Regulatory Affairs Specialist that will support product development teams to deliver regulatory inputs, strategies, reports and other design control deliverables. Prepare Quality Assurance/Regulatory reports and present status in review meetings...Immediate start
- ...caps, captive carrier limitations, or opaque lead structures? We are expanding our network of established financial protection specialists. This 1099 entrepreneurial partnership is tailored for self-starting professionals who want to maximize their earning potential by...Contract workWork at officeImmediate startRemote work
$114.91k - $141.95k
...'ll do:As a Compliance Assistant Manager you'll be a subject matter expert and provide advice, oversight and guidance related to regulatory compliance risks, control effectiveness, root cause analysis, and issue review and validation. You'll provide leadership and direction...Full timeContract work$86k - $114k
...to the United States and its allies. Operating in a fast-growing, high-impact environment, we take creative ownership of complex regulatory matters to build and manage efficient, top-tier compliance processes. We are deeply passionate about the law and policy of defense...Full timeFor contractorsWork experience placementImmediate start- Company DescriptionAt the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight...
$66.1k - $118.3k
...able to communicate research and data findings in a meaningful way. You will be responsible for monitoring internal and external regulatory audits. And you will be expected to monitor changes in requirements to mitigate risks and achieve compliance. You’ll enjoy the flexibility...Work experience placementLocal areaRemote work$99.7k - $152.08k
The Sr. Export Compliance Specialist supports the company’s export compliance program to ensure compliance with U.S. export control regulations and protect sensitive technology and information. This role partners cross-functionally to provide practical compliance guidance...Permanent employmentFull timeFor contractorsCasual workWork at office- Licensed Loan Officer All In Bound Leads | No Cold Calling | Make Great Money | Have a Career Do you have your NMLS CA-DOC license? Do you have at least one year of experience selling home loans? Would you like to build a career with a stable and financially...Work at officeImmediate start
$38.46 - $40.87 per hour
...THIS POSITION WILL BE LOCATED IN WILIMINGTON, CA 90744 Ensure compliance with LIHTC, HUD, and other owner, investor, lender, and regulatory agency requirements. Audit move‑in, recertification, and eligibility files; prepare and submit required compliance reports; track...Hourly payFull timeWork at officeMonday to FridayFlexible hours$15.5 per hour
Cleaning & Veterinary Animal Hospital Care Nursing Staff (Training).NEW job posting beginning 10/1/2025 One additional job now available.We need to hire another fabulous hard working person as ... Show more Full-time To autonomously maintain and operate equipment, supplies...Hourly payFull timeWork from homeNight shift- ...HIGH-LEVEL OVERVIEW The Senior Trade Compliance Specialist is responsible for ECCN and HTS classification of technology products... ...flows, and FAQs • Conduct compliance audits and prepare regulatory reporting • Prepare metrics, KPIs, and reporting on classification...
- ...responses and that related corrective actions are completed Review consumer communications and marketing/advertising materials for regulatory compliance Assist in implementing, administering, and enhancing the company’s issues management program and tracking remediation...Full timeLocal areaRemote workWork visa
- ...leading technology firm in California is seeking a Trade Compliance Specialist responsible for the ECCN and HTS classification of technology... ...U.S. Export Control Laws, the ability to navigate intricate regulatory standards, and proficient technical skills in analyzing...
$23 - $25 per hour
...attention to detail, and the ability to identify risks, recommend practical solutions, and support a culture of accountability, regulatory readiness, and continuous improvement. About Us At Alleviate Financial Solutions , we’re transforming lives every day by offering...Hourly payFull timeFixed term contractWork at officeLocal areaMonday to FridayShift work$30 - $45 per hour
We are seeking a skilled Labor Compliance Coordinator to join our team. In this role, your aim is to ensure employees are compensated accurately and promptly. Your responsibilities will include processing timesheets, updating records, overseeing payroll payments, and answering...Hourly pay
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