141 Results for

Regulatory Affairs Jobs in Boyle Heights, CA

Jobs

Los Angeles, CA7 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.

New!

Los Angeles, CA2 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, CA1 day ago

Remote

$85,000–$145,000 Per Year

Functions as an internal consultant to colleagues throughout City National Bank (CNB) related to operational compliance issues and concerns, utilizing their internal and external organizational agility to ascertain and deliver sound interpretation and advice. Benefits and PerksAt City National, we strive to be the best at whatever we do, including the benefits and perks we offer our colleagues including:Comprehensive healthcare coverage, including Medical, Dental and Vision plans, available the first of the month following start date.

New!

Irvine, CAToday

$180,000–$260,000 Per Year

Exercises independent judgment in resolving highly complex, systemic, and enterprise level problems with significant regulatory, financial, and reputational impact Regularly consults and advises senior leadership and Group / Board level stakeholders on Quality strategy, risk, compliance posture, and organizational capability. This role provides scientific leadership, ensures method robustness and compliance, drives harmonization across sites, and supports product lifecycle needs—including development, validation, transfer, troubleshooting, and regulatory submissions of analytical methods and specification.

New!

Newport Beach, CA1 day ago

The firm is known for its strong presence in fixed income markets and its growing focus on alternative investments and private fund strategies. A globally recognized investment management organization is seeking a detail-oriented and motivated Compliance Consultant for a temporary opportunity within its Legal and Compliance team.

New!

Los Angeles, CA1 day 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) .

New!

Santa Clarita, CAToday

$38.46–$43.27 Per Hour

We’ve been serving the professional beauty industry with salon-quality hair care products, styling tools and professional hair color through our family of brands including Paul Mitchell, MITCH, Awapuhi Wild Ginger, Tea Tree, Paul Mitchell Tools, Neuro, The Demi, Paul Mitchell the Color, Blonde, and Color XG. Reporting to the Director, Regulatory Affairs, the Regulatory Affairs Specialist will be responsible for supporting registration/regulatory needs to maintain and further develop the regulatory capability, to support global innovation projects, and to address business issues to meet business goals.

New!

Los Angeles, CA1 day ago

Remote

$180,000–$220,000

Strategic Scientific Engagement & Insight Generation: Establishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators working in multiple system atrophy. This role serves as a strategic pre-launch scientific partner to external experts and internal stakeholders, generating high-quality, actionable insights that inform evidence strategy, disease education, portfolio decision-making, and launch readiness.

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.

New!

Los Angeles, CA5 days ago

$45–$55.53 Per Hour
Temporary
Contractor
Full-time

This position independently manages full-cycle investigations from intake through closure, develops investigative strategies, prepares evidentiary packages for regulatory or law enforcement referral, and provides clinical and operational insight into healthcare billing patterns and provider behaviors. Strong understanding of coding and reimbursement structures (including Current Procedural Terminology (CPT), Healthcare Common Procedure Coding Systems (HCPCS), International Classification of Diseases (ICD-10)), medical billing, and claims review processes.

Irvine, CA30+ days ago

$80,000–$100,000 Per Year

Physical: Generally, may require some reaching, bending, stooping, squatting, crawling, kneeling, pushing, pulling, lifting, carrying up to 20 pounds, finger dexterity, repetitive motions, standing, walking, sitting, hearing, visual acuity, and color vision. Work with RA Leadership and other members of the RA team to set strategy for regulatory approval to introduce new products to market, evaluate regulatory requirements and prepare regulatory submissions.

Orange, California25 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

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, California12 days ago

Responsibilities: Under the general direction of the Assistant Director of Clinical Research Operations of the UCI Center for Clinical Research (CCR), the Manager of Regulatory Affairs and Quality Assurance is responsible for all clinical research regulatory and quality assurance operational matters in fulfilling the mission of CCR under the University of California, Irvine - School of Medicine and the overall UC Irvine Health enterprise. *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

$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.

Huntington Beach, California27 days ago

$90,000–$120,000

Without a written agreement signed by an officer of SprintRay: a) SprintRay does not accept resumes from recruiting agencies, headhunters, or any other party expecting payment in the event SprintRay speaks with or hires a candidate from such submitted resume; b) SprintRay is not responsible for any fees related to unsolicited resumes or related Terms of Service, and c) Unsolicited resumes received will be considered the property of SprintRay and will be processed accordingly. Whether we’re building next-generation AI tools, designing new materials, or supporting our customers on the front lines, we’re united by the same passion—transforming digital dentistry and having fun while we do it.

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

$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.

Westminster, CA19 days 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

$38–$45

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.

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!

TORRANCE, CA6 days ago

Full-time

This role will support Class I and Class II medical device programs, including technical documentation, design history files, change control, risk management, supplier documentation, labeling review, customer regulatory requests, and audit readiness. Experience with Class II medical devices, 510(k) support, IEC 60601-1, EU MDR technical documentation, or customer-driven regulatory submissions is highly preferred.

Santa Clarita, CA30+ days ago

The Regulatory & Quality Affairs Manager ensures all facilities and or business entities maintain full compliance with all applicable state & federal regulatory requirements and guidelines for the marketing, sales, warehousing and distribution of the company’s products in their respective target markets. Ensure that known compliance risks (via internal/external audits, changes in regulations, changes in business structure/products) are mitigated via quality/compliance plans.

Cerritos, CA7 days ago

Noodle & Boo is seeking a highly organized, scientifically rigorous, and detail-oriented Manager, Product Integrity, Regulatory & Scientific Affairs to support the day-to-day execution of formula governance, regulatory documentation, product compliance, technical recordkeeping, claims substantiation, COA review, and manufacturing quality consistency across our premium baby, maternity, and family care portfolio. Reporting to the Founder and ultimately the VP Product / Chief Product Officer, this role is cross-functional and operationally important, but remains a manager-level, hands-on role focused on execution, documentation control, quality follow-up, and compliance support.

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.

Beverly Hills, CA30+ 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 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.

Irvine, California7 days ago

The Supervisor, Study Startup and Regulatory independently directs and supervises the day-to-day management of critical startup and regulatory requirements for clinical research within ASCC and has primary responsibility for overseeing startup and regulatory affairs coordinators who are responsible for creating, negotiating, and monitoring budgets for clinical trials and grants, and regulatory coordination activities for UCI Alpha Clinic. *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.

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.

Westminster, CA30+ 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.

New!

Irvine, CAToday

$180,000–$260,000 Per Year

This role provides scientific leadership, ensures method robustness and compliance, drives harmonization across sites, and supports product lifecycle needs—including development, validation, transfer, troubleshooting, and regulatory submissions of analytical methods and specification. The Director of Central Analytical Services is a senior leader responsible for establishing, governing, and optimizing analytical strategy, technical capabilities, and laboratory performance across a network of sterile pharmaceutical manufacturing sites.

New!

Chino, CA6 days ago

$96,239–$112,000 Per Year

The FSQA Senior Specialist - Meat guarantees excellence and uniformityacross all INO facilities in terms of workflow and regulatory adherence, utilizing extensive relevant experience to facilitate internal and vendor program enhancements, as well as to instruct, train, develop, and mentor fellow Associates. In-N-Out Burger's menu has remained the same since 1948, and we have maintained a simple philosophy - serve only the highest quality product, prepare it in a clean and sparkling environment, and serve it in a warm and friendly manner.

Los Angeles, CA14 days ago

Remote

Full-time

Established in 2010, with a business plan no longer than a paragraph, Kitsch has grown from door to door sales to selling products in over 27 countries across 20,000 retail locations worldwide. Develop and maintain a master labeling matrix by SKU and marketplace covering required warnings, symbols, barcodes, language, and regulatory marks.

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!

Chino, CA6 days ago

$96,239–$112,000 Per Year

Position requires frequent lifting, walking, reaching, standing, climbing, stooping, bending, kneeling, working near moving mechanical parts* Cold working conditions: Ability to withstand prolonged work assignments in temperatures as low as 36 degrees Fahrenheit* Frequently exposed to wet humid conditions (non-weather)ABOUT In-N-Out BurgerIn-N-Out Burger was founded in 1948 by Harry and Esther Snyder in Baldwin Park, California, and remains privately owned and operated. The FSQA Senior Specialist - Meat guarantees excellence and uniformity across all INO facilities in terms of workflow and regulatory adherence, utilizing extensive relevant experience to facilitate internal and vendor program enhancements, as well as to instruct, train, develop, and mentor fellow Associates.

Seal Beach, California11 days ago

Responsibilities: Serves as an essential link between Dendreon Medical Affairs and healthcare professionals (HCPs) and non-HCPs (including patients and payors); assisting with the appropriate dissemination of scientific information, while continuously monitoring enquiry trends and metrics and proactively identifying unmet content needs and product trends to the wider Dendreon audience. Recognizes and obtains pertinent patient level data on, and accurately transmits, adverse events or product complaints to appropriate internal pharmacovigilance (PV) department within required timelines (within 24 hours of awareness); maintains a record of all external Medical Information interactions via the IRMS database.

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, CA29 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.

Los Angeles, CA30+ days ago

$260,000–$300,000 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. Prior MSL leadership experience required, with demonstrated leadership ability, skilled in strategic thinking, building alignment, innovative problem-solving, and driving team performance.

Los Angeles, CA30+ 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.

Fullerton, CA30+ 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.

New!

Torrance, California6 days ago

Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). US Benefits Statement: Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off.

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, CA30+ days ago

Remote

$180,000–$225,000 Per Year

This Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

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.

Irvine, California11 days ago

$108,100–$141,000 Per Year

The Director independently manages complex projects involving the design, implementation, and continuous improvement of academic nursing programs across all degree levels (undergraduate, graduate, and doctoral) in addition to development and administration of non-clinical undergraduate pathways, such as pre-nursing programs, ensuring program integrity, student success, faculty development support, and regulatory compliance. At the UCI Sue & Bill Gross School of Nursing, we dedicate ourselves to the education of nursing professionals who improve patient care and promote community and population health, locally and globally, and we strive to produce leaders in research, education, and clinical practice who will champion collaborative, compassionate, and interdisciplinary evidence-based practice.

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.

Los Angeles, CA30+ days ago

$220,000–$240,000 Per Year

This position will report to the Group VP Program Management and will act as the Global Product Team (PT) Manager responsible for ensuring effective global launch, life cycle management and product strategy for multiple late stage and commercial products. 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.

Pasadena, CA30+ days ago

$160,000–$180,000 Per Year

This position will report to the Director of Compliance and will work closely with members of the Legal, Commercial, Medical Affairs, Regulatory, Quality teams to promote awareness and understanding of positive ethical principles and ensure continuous suitability and alignment of compliance program framework and controls relevant laws and company's goals. 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.

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Regulatory Affairs Jobs in Boyle Heights, CA

Quality Systems & Regulatory Manager Jobot

Documentation Specialist Vaco LLC

Compliance Specialist Senior Wealth Management City National Bank

Director, Central Analytical Services B. BRAUN MEDICAL INC

(Contract - up to $60) Investment Compliance Consultant ProPivotal

Compliance Officer-Lending City National Bank

Specialist, Regulatory Affairs John Paul Mitchell Systems

Senior Medical Science Liaison Movement Disorders - West Lundbeck

Regulatory Affairs Specialist (FDA, DEA ) BaRupOn LLC

SIU Clinical Healthcare Fraud Investigator III Solugenix Corp

Regulatory Affairs Specialist Nihon Kohden

Regulatory Affairs Coordinator University of California, Irvine

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

Regulatory Affairs & Quality Assurance Manager University of California, Irvine

Specialist, Regulatory Affairs THV Edwards Lifesciences

Regulatory Affairs and Quality Assurance Specialist SprintRay

Senior Specialist, Regulatory Affairs Surgical Edwards Lifesciences

Senior Manager, Regulatory Affairs TMTT Edwards Lifesciences

Utility Regulatory Affairs Senior Advisor Southern California Edison

Regulatory Affairs Manager Huisong Pharmaceuticals

Coord 3, Regulatory Affairs Pyramid, Inc

REGULATORY AFFAIR SPECIALIST Broadata Communications

Regulatory Affairs Manager CEDENT

Manager, Product Integrity, Regulatory & Scientific Affairs Noodle & Boo, Inc.

Director, Medical Affairs (Cardiometabolic) Arrowhead Pharmaceuticals

SVP, Legal & Business Affairs Avalon

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

Supervisor, Study Startup and Regulatory University of California, Irvine

Manager, Regulatory V 26-00077 Alura Workforce Solutions

Regulatory Compliance Senior Advisor Southern California Edison

Director, Central Analytical Services B. BRAUN MEDICAL (US) INC

Senior FSQA Specialist In-N-Out Burgers

Amazon Compliance Specialist Kitsch LLC

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

Senior FSQA Specialist In-N-Out Burger - Corporate

Medical Information Specialist Dendreon Corporation

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

Director of Compliance #0204CG Keller Executive Search

Senior Director, Field Medical Lead Arrowhead Pharmaceuticals

Senior Director, Global Scientific Communications and Publications - Remote Agios Pharmaceuticals

Food Safety Compliance Specialist Motive Companies

Head of Engineering (Multidisciplinary) – SMR / MMR Programs BaRupOn LLC

Specialist, Quality Compliance (Label) Herbalife

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

Senior Medical Science Liaison/Medical Science Liaison – Southwest Region Beam Therapeutics

Executive Director RCFE Brookdale Senior Living

Director of Academic Nursing Administration University of California, Irvine

Experienced Clinical Research Coordinator Greater Los Angeles Veterans Research and Education Foundation

Director, Commercial Program Management Arrowhead Pharmaceuticals

Senior Manager, Healthcare Compliance Arrowhead Pharmaceuticals

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