116 Results for

Regulatory Affairs Jobs in Carson, CA

Jobs

New!

Los Angeles, CA4 days ago

Remote

$183,549–$275,324 Per Year

The current base salary range for this position is expected to be between $183,549 – $275,324 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. As a key cross-functional partner, the Medical Director collaborates closely with Commercial, Clinical Development, Regulatory, and Market Access teams, among others, to shape brand and portfolio strategy, integrating real-world evidence and external expert perspectives.

New!

Los Angeles, CA4 days ago

$90,000–$120,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. They’re looking for a tech-savvy and detail-oriented Quality Systems & Regulatory Manager to lead food safety systems, labeling accuracy, customer compliance documentation, and cross-functional audit readiness.

Los Angeles, CA7 days ago

$30–$35

Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. Vaco by Highspring values a diverse workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply.

New!

Los Angeles, CA4 days ago

Remote

$229,562–$344,342 Per Year

The role oversees a high-impact team and partners cross-functionally and externally to drive an integrated publications and scientific communications strategy, translating complex data into compelling evidence that supports clinical adoption, informs healthcare decision-making, and differentiates the company’s portfolio globally. Agios Pharmaceuticals is searching for a dynamic Senior Director, Global Scientific Communications and Publications expert to join our Global Medical Affairs team and lead a high-functioning communications/publications/congress team.

New!

La Habra, CA2 days ago

$112,031–$168,046

Additionally, if the nursing requirements listed below are not met, an individual may be placed in the Administrator role without them; however, in the absence of these qualifications, there must be a designated Registered Supervising Nurse at the clinic who does possess these qualifications: Must be full-time employee of the Company and available to clinic staff during time clinic is open. ÃÂÃÂ· Continuously monitor to ensure that a safe and sanitary physical environment is maintained throughout the facility; that all equipment is maintained and functions properly; and that adequate and appropriate inventory levels of all supplies are available and used correctly.

New!

Los Angeles, CA3 days ago

Remote

$111,408–$189,738 Per Year

Advanced knowledge of banking compliance laws and regulations, as related to mortgage lending, and mortgage banking operations (Examples include but are not limited to: ECOA/Regulation B, FCRA , Flood Disaster Protection Act, Truth in Savings Act, SCRA, HMDA, RESPA, TILA, Regulation O, Regulation W. Compliance Officer Senior - Mortgage is responsible for managing and maintaining assigned areas of the compliance program covering U.S. Mortgage Banking including monitoring business area compliance with applicable laws and regulations, ensuring controls are in place to mitigate compliance risk.

Los Angeles, CA14 days ago

This leader serves as the senior clinical authority for NAM education, ensuring programs meet the needs of practicing clinicians while supporting business priorities, product adoption, and long term customer trust. • Oversee planning and execution of clinical educational events (e.g., courses, workshops, symposia, webinars), ensuring end-to-end operational excellence (logistics, faculty coordination, attendee experience) and alignment to learning objectives.

Irvine, CA30+ days ago

$60,000–$76,000

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. The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements.

Irvine, CA30+ days ago

BaRupOn LLC is seeking a highly experienced Director of Licensing & Regulatory Affairs to lead all regulatory strategy, licensing execution, and compliance activities for its Small Modular Reactor (SMR) and Micro Modular Reactor (MMR) programs in the United States. The ideal candidate brings deep, direct NRC engagement experience, a thorough command of U.S. nuclear regulatory frameworks, and the leadership ability to build and manage a high-performing regulatory team in a fast-moving, mission-driven environment.

Orange, California7 days ago

Proven organizational skills and attention to detail; ability to multi-task, prioritize a complex and dynamic workload, meet rigid deadlines despite interruptions, frequent workload changes and competing demands, and achieve high productivity/quality within short time frames; skill in working independently, taking initiative and following through on assignments and ability to work as part of a team. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.

Irvine, CA30+ days ago

$92,000–$130,000 Per Year

Prepare, compile, and support global regulatory submissions for assigned products, including: U.S. submissions (e.g., 510(k)s, IDEs, PMAs, PMA supplements, annual reports) EU submissions under the Medical Device Regulation (MDR) (e.g., Technical Documentation, Design Dossiers, STEDs, clinical evaluation documentation, and responses to Notified Body questions) Support CE marking activities and interactions with Notified Bodies for Class III implantable devices. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives.

Irvine, CA30+ days ago

$72,000–$102,000 Per Year

Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives. + Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or reporting to management.

Irvine, CA30+ days ago

$145,000–$205,000 Per Year

Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives. Includes representing the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including providing alternatives for meeting regulatory requirements and resolving complex conflicts between those requirements and development issues.

Irvine, CA30+ days ago

$90,000–$127,000 Per Year

Determine and discern detailed requirements on mid-to-large scale projects to establish the project deliverables and develop the project management plan, and manage changes to the project scope, schedule, and costs to keep the project management plan updated and reflective of authorized project changes. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients’ lives.

Irvine, CA30+ days ago

$50–$54 Per Hour
Contractor

Strict attention to detail Ability to interact professionally with all organizational levels Ability to manage competing priorities in a fast paced environment Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects Ability to build productive internal/external working relationships Bachelor's Degree or equivalent in scientific discipline (e.g., Biology, Microbiology, Chemistry) 5-7 years of experience requiredOur client is a leading Medical technology Industry and we are currently interviewing to fill this and other similar contract positions. Coursework, seminars, and/or other formal government and/or trade association training required Proven expertise in Microsoft Office Suite including Word, PowerPoint and Excel Good written and verbal communication skills and interpersonal relationship skills Good problem-solving, organizational, analytical and critical thinking skills Solid knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices Solid knowledge and understanding of global regulatory requirements for new products or product changes.

New!

Westminster, CA1 day ago

In this job, you will engage with business units across SCE to develop strategies, business cases, and regulatory deliverables in support of key SCE objectives that require engagement with external regulatory agencies such as the California Public Utilities Commission. You will lead the development of components in the regulatory process, including the full lifecycle from development of testimony, discovery and data requests, hearings, workshops, comments, and final decisions.

Santa Ana, California30+ days ago

$35–$40

About Huisong:Founded in 1998, Huisong Pharmaceuticals specializes in the R&D and manufacturing of premium-quality natural ingredients for world-leading companies in the pharmaceutical, nutraceutical, food & beverage, and personal care industries. Today, Huisong Pharmaceuticals is a global operation with an extensive and dynamic product portfolio of natural products and ingredients, remaining firm in its values of "Nature, Health, Science", and continues to advance the world of medicine and nutrition for the well-being of humanity.

Los Angeles, CA30+ days ago

$230,000–$260,000 Per Year

Reporting to the Executive Director, Medical Affairs Strategy, this role plays a central part in shaping the scientific narrative, supporting launch readiness, and translating complex clinical data into meaningful insights that inform commercial strategy while preserving medical integrity. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Los Angeles, CA30+ days ago

$76,800–$100,800 Per Year

The Senior Analyst, Government Affairs is a contributor and owner of mission-critical workflows to communicate proposed and enacted legislation, regulations, bulletins, and other regulatory guidance to impacted teams. Support the Government Affairs Counsel with overseeing trade association committees, covering hearings and meetings as assigned by the Government Affairs Counsel and summarizing takeaways for our teams.

Beverly Hills, CA20 days ago

Full-time

This position operates at the center of deal-making and project execution, leading complex negotiations, advising on contractual matters, and ensuring agreements are structured and executed effectively across Avalon’s US slate. The SVP, Business Affairs, will play a central role across Avalon’s US operations, supporting the talent management and television production business across a wide range of film, television, and digital projects.

Los Angelas, CA30+ days ago

Full-time

Homeboy Industries is the largest gang rehabilitation and re-entry program in the world, providing hope, training, and support to formerly gang-involved and previously incarcerated people, allowing them to redirect their lives and become contributing members of our community. The GAO will write and submit public grant proposals, monitor compliance and reporting requirements, build relationships with key stakeholders to represent Homeboy Industries in grantor monitoring meetings and trainings.

Los Angeles, CA30+ days ago

$180,000–$210,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. The Associate Director serves as a subject matter expert in electronic submissions (eCTD), publishing systems, and regulatory operation infrastructure, driving submission excellence, process optimization, compliance readiness, and system innovation across the Regulatory organization.

Cypress, CA7 days ago

$28.85–$32.50 Per Hour

This role supports labeling and regulatory activities for plant‑based products, contributes to product and process development, including new technologies, and performs general R&D tasks such as product maintenance and new product development. Food labeling, regulatory, food compliance, Research and Development, R&D, Food science, allergen statements, Nutrition Facts, Food product labels.

Pomona, CA30+ days ago

This role will focus on evaluating emerging grid technologies and architecture through financial and economic analysis, supporting investment decisions, and ensuring alignment with regulatory requirements. The position will play a key role in developing cost-benefit analyses, financial models, and business cases to support strategic planning and grid modernization initiatives.

El Segundo, CA7 days ago

This role sits at the intersection of childrens safety, artificial intelligence, and digital product innovation, offering a unique opportunity to influence how AI-enabled and connected products are designed, evaluated, and launched responsibly. This contract role is ideal for professionals eager to apply policy, legal, and technical knowledge to real-world AI and digital safety challengeswhile helping create safer, more trusted experiences for children.

Westminster, CA14 days ago

Excellent cross functional collaboration skills, with the ability to lead without authority and align diverse stakeholders* Advanced analytical, problem solving, and strategic thinking capabilities* Exceptional written and verbal communication skills, including executive level briefings. The role influences enterprise-wide decision making by interpreting regulatory requirements, advising senior leaders, and driving proactive compliance strategies that reduce exposure and support business objectives.

Irvine, CA30+ days ago

The Government Relations Lead will serve as BaRupOn's primary external voice with the U.S. Nuclear Regulatory Commission (NRC), Department of Energy (DOE), Congress, state agencies, and industry coalitions — building the relationships and policy positioning that enable BaRupOn's programs to advance through the U.S. regulatory and political landscape. BaRupOn LLC is seeking an experienced and strategically minded Government Relations & Partnerships Lead to own the company's engagement with federal, state, and local stakeholders across its Small Modular Reactor (SMR) and Micro Modular Reactor (MMR) programs in the United States.

New!

Anaheim, CA5 days ago

We are looking for a strategic operations professional who understands the complexities of the medical device industry, including Quality Assurance (QA), Service Level Agreements (SLAs), FDA/ISO compliance, and ERP-driven inventory management. The ideal candidate is a highly analytical problem solver, an advanced Odoo user, and someone who thrives in fast-paced environments where accuracy, accountability, and continuous improvement are essential.

Irvine, CA30+ days ago

BaRupOn LLC is seeking an experienced and strategically minded Head of Project Development / Program Director to lead the end-to-end planning, execution, and delivery of its Small Modular Reactor (SMR) and Micro Modular Reactor (MMR) projects in the United States. The ideal candidate is a proven large-scale nuclear project leader who has navigated the full complexity of U.S. nuclear project development — someone who can manage multidisciplinary teams with equal fluency across the technical, regulatory, and commercial dimensions of advanced reactor deployment.

Los Angeles, CA11 days ago

$145,000–$180,000

Our client is a well-capitalized early-stage venture developing a premium West Coast point-to-point carrier focused on connecting California metros to mountain resort and entertainment-driven destinations. This role calls for a compliance professional who combines technical aviation regulatory depth with the diplomatic skill to engage federal and state agencies while building internal frameworks from a clean slate.

Fullerton, CA13 days ago

The Global Food Safety & Quality Compliance Specialist II is responsible for supporting the oversight and execution of food safety and quality management systems across an international network of manufacturing facilities, co-manufacturers, and supply chain partners. This role ensures compliance with food safety regulations across multiple global markets and helps drive continuous improvement initiatives related to food safety culture, regulatory compliance, and quality management systems.

Irvine, CA30+ days ago

The ideal candidate brings extensive multidisciplinary engineering experience in the U.S. nuclear sector, a proven track record leading complex advanced reactor or SMR programs, and the executive presence to represent BaRupOn's engineering organization internally and externally. This person will work in close partnership with the CTO, CNO, Director of Licensing, and project leadership to ensure every engineering deliverable is technically sound, schedule-aware, and fully aligned with NRC requirements.

Irvine, CA30+ days ago

The ideal candidate brings deep hands-on experience in reactor physics and core design for advanced or non-light water reactors, a strong command of U.S. nuclear regulatory frameworks, and the technical leadership ability to guide a growing team of physicists and engineers in a fast-paced, mission-driven environment. BaRupOn LLC is seeking a highly experienced Lead Reactor Physicist / Core Design Lead to own the reactor physics and core design program for its Small Modular Reactor (SMR) and Micro Modular Reactor (MMR) initiatives in the United States.

Los Angeles, California30+ days ago

$21.06–$31.40

The CRC supports multiple Phase II-IV clinical trials across a variety of disciplines and investigators which may be sponsored by federal agencies including NIH or DOD and pharmaceutical sponsors or CRO’s. Schedule and attend all Site Initiation Visits, Monitoring Visits, Close-Out Visits etc. for all assigned studies/or when asked to attend by the Lead Clinical Coordinator.

Irvine, CA30+ days ago

Full-time

With our core lab already established in Stuttgart, this role will focus on extending our testing capacity, strengthening our infrastructure, and building the team that will support design verification focused on mechanical testing, R&D, and post‑market surveillance. As we continue to scale our U.S. headquarters in Irvine and strengthen our global operating model, we are seeking a Testing Manager to help lead the expansion of Kardion’s product testing capabilities in Irvine.

New!

Los Angeles, CA3 days ago

Remote

$264,000–$290,000 Per Year

The Payor and Health Systems Liaison leads high impact clinical, scientific, and population health engagement with external access stakeholders, including Payers, Group Purchasing Organizations (GPOs), Community Aggregators, and Integrated Delivery Networks (IDNs), while ensuring strong integration between Medical Affairs, HEOR, and Market Access strategy. They will develop and cultivate relationships with key decision-makers and other influencers in managed care organizations, government programs, employers, hospital systems and product distribution companies, to support appropriate patient access and evidence-based utilization for our client’s products.

Los Angeles, CA30+ days ago

Full-time

In the past few years, Woodcraft has expanded its menu of services beyond traditional afterschool programs and summer camps to include early learning, environmental and social justice, college access, and inclusion services for youth with intellectual and developmental disabilities. Continuously at the forefront of expanded learning opportunities, Woodcraft Rangers has a rich history of making a significant impact in the greater Los Angeles area, believing that all youth are innately good, deserve the opportunity to realize their full potential, and should be an active participant in defining their own path.

Los Angeles, CA30+ days ago

$42–$45.70 Per Hour

This position is ideal for candidates with strong experience in safety data analysis, pharmacovigilance systems, and database reporting, particularly those who have worked with safety databases and reporting tools in regulated environments. Critical Skills & Experience (Highly Preferred)Strong experience with safety data analysis and reporting tools (Business Objects strongly preferred).

Long Beach, CA30+ days ago

Positions will be assigned to specific sections within the department, including Capital Development, Projects & Construction, Business Management, and Maintenance & Operations, and report to the respective Section Supervisor in support of medical center tasks. Must be able to communicate effectively both in writing and verbally with a variety of contractors, management officials, vendors, Contracting Officers at Long Beach staff, and meet stated deadlines.

Los Angeles, CA30 days ago

Remote

$185,000–$215,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

Los Angeles, California11 days ago

Remote

$77,000–$143,000 Per Year

The incumbent is responsible for monitoring issues remediation strategy for compliance identified issues and ensuring issues are closed in a manner which both adheres to the regulatory requirements while assisting business areas with implementing corrective actions or procedural changes, and applying a risk-based approach to remediation strategies. Advanced knowledge of banking and consumer compliance laws and regulations, as related to lending and bank operations (Examples include but are not limited to: ECOA/Regulation B, FCRA, Flood Disaster Protection Act,, MLA, SCRA, RESPA, TILA, TRID) .

Santa Monica, CA30+ days ago

Full-time

Drives sales and marketing efforts in collaboration with the community sales leader to meet or exceed occupancy or revenue targets by developing new business, generating leads, and building strategic relationships. Recognized by Newsweek in 2024 and 2025 as one of America's Greatest Workplaces for DiversityBrookdale Ocean House is seeking a polished, professional Executive Director to lead our premier oceanfront assisted living community.

Rosemead, CA30+ days ago

This program represents a high level of investment by the enterprise as participants rotate through a variety of directed assignments and improves the development of individuals for potential placement in a leadership role after the program. The program is designed to provide participants with cross-functional and customized work experiences that develop leadership skills for future leadership positions within the company.

Pasadena, California30+ days ago

Our teams of experienced, multi-cultural professionals help guide businesses and community members on both sides of the Pacific looking to explore new markets and create new opportunities, and our sustained growth and expertise in industries like real estate, entertainment and media, private equity and venture capital, and high-tech help build sustainable businesses and expand our associates’ potential for career advancement. The ideal candidate will bring deep expertise, strategic vision, and a results-oriented mindset to help Treasury achieve best-in-class governance, operational efficiency, and regulatory alignment as we navigate this exciting phase in our continued growth and evolution.

Santa Ana, California10 days ago

$88,452–$115,293 Per Year

They will act as the central interface between Commercial, Technical (R&D), Operations, Quality/Regulatory, and Business Support teams to define requirements, prioritize developments, and drive successful commercialization and ongoing optimization of services and or applications-based products. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world’s biggest health challenges.

Torrance, CA30+ days ago

Full-time

Proficiency in quality tools and methodologies, including Supplier Assessments, First Article Inspections (FAI), Failure Modes and Effects Analysis (FMEA), 8D Problem Solving, Root Cause Analysis, Corrective and Preventive Actions (CAPA), Mistake Proofing and Process Control. Minimum 5 years of relevant experience in engineering, quality assurance, or manufacturing supplier quality in regulated manufacturing environment (cosmetics or OTC drugs a plus).

Los Angeles, CA17 days ago

Remote

$268,000–$295,000 Per Year

Demonstrated leadership skills (proactive, strategic, creates a highly accountable team culture, provides clear direction), project management and organizational skills, with the ability to evaluate competing priorities to arrive at an appropriate decision. Oversees execution of stakeholder engagement strategy across regional and community healthcare providers, including academic institutions and community centers across the aligned region to ensure timely and accurate scientific communication.

Irvine, CA30+ days ago

$183,000–$490,000 Per Year

The Executive Medical Director is responsible for the safety strategy for solid tumors late-stage oncology portfolio, and to supervise, manage and mentor the safety physicians (Group MDs, Senior MDs and medical directors) and supporting the Solid Tumor in the Oncology TA. Clinical Development, Regulatory Affairs, Medical Affairs), as needed, to ensure the successful development, design, and implementation of comprehensive safety assessment to support both study participants in asset development programs and patients on the marketed product.

Santa Ana, CA16 days ago

$173,000–$195,000 Per Year

The ideal manager combines deep technical expertise with effective leadership skills, ensuring high-quality output, strong team performance, and timely execution across multiple projects. The Electrical Design Engineering Manager serves as a critical leader within the R&D organization, responsible for guiding and developing the electrical engineering team while driving all electronic design efforts.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Regulatory Affairs job opportunities. Plus, receive relevant job recommendations in your inbox.

Regulatory Affairs Jobs in Carson, CA

Jobs

Medical Director, Global Medical Affairs - RemoteAgios Pharmaceuticals

Quality Systems & Regulatory ManagerJobot

Documentation SpecialistVaco LLC

Senior Director, Global Scientific Communications and Publications - RemoteAgios Pharmaceuticals

Dialysis Facility AdministratorU.S. Renal Care

Compliance Officer Senior-Mortgage OriginationCity National Bank

Senior Director, Clinical Education and EventsDentsply Sirona

Regulatory Affairs Specialist (FDA, DEA )BaRupOn LLC

Director of Licensing & Regulatory Affairs (SMR / MMR Programs)BaRupOn LLC

Regulatory Affairs CoordinatorUniversity of California, Irvine

Senior Specialist, Regulatory Affairs SurgicalEdwards Lifesciences

Specialist, Regulatory Affairs THVEdwards Lifesciences

Senior Manager, Regulatory Affairs TMTTEdwards Lifesciences

Senior Analyst, Project Management, Regulatory Affairs SurgicalEdwards Lifesciences

Coord 3, Regulatory AffairsPyramid, Inc

Utility Regulatory Affairs Senior AdvisorSouthern California Edison

Regulatory Affairs ManagerHuisong Pharmaceuticals

Director, Medical Affairs (Cardiometabolic)Arrowhead Pharmaceuticals

Senior Analyst, Government AffairsOscar

SVP, Legal & Business AffairsAvalon

Government Affairs Grant OfficerHomeboy Industries

Associate Director, Global Regulatory Operations (Regulatory Submissions and Publishing)Arrowhead Pharmaceuticals

Labeling & Regulatory Associate - FoodTriCom Quest

Manager, Regulatory V 26-00077Alura Workforce Solutions

AI Digital Safety, Regulatory and Compliance AnalystApollo Professional Solutions

Regulatory Compliance Senior AdvisorSouthern California Edison

Government Relations & Partnerships Lead (SMR / MMR Programs)BaRupOn LLC

Inventory & Logistics SpecialistArgus Medical Management, LLC

Head of Project Development / Program Director (SMR)BaRupOn LLC

Director of Compliance #0204CGKeller Executive Search

Food Safety Compliance SpecialistMotive Companies

Head of Engineering (Multidisciplinary) – SMR / MMR ProgramsBaRupOn LLC

Lead Reactor Physicist / Core Design Lead (SMR / MMR Programs)BaRupOn LLC

Experienced Clinical Research CoordinatorGreater Los Angeles Veterans Research and Education Foundation

Testing ManagerKardion

Senior Director, Payor and Health Systems LiaisonTaylor Strategy Partners

Senior Director of Enterprise Risk & Legal OperationsWoodcraft Rangers

Drug Safety AnalystConnexion Systems + Engineering

DrafterTerrestris Global Solutions

District ManagerTaylor Strategy Partners

Compliance Officer-LendingCity National Bank

Executive Director RCFEBrookdale Senior Living

2026 MBA Leadership Development Program AssociateSouthern California Edison

Treasury GovernanceEast West Bank

Product Manager- Bioprocessing ServicesFujifilm

Supplier Quality Manager-Torrance, CAPrime Matter Labs

Senior Director, Regional Medical Science LiaisonTaylor Strategy Partners

Executive Medical DirectorAbbVie

Electrical Design Engineering ManagerNihon Kohden Orange Med

Resume Resources