134 Results for

Regulatory Manager Jobs in Beverly Hills, CA

Jobs

Orange, California30+ 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.

Los Angeles, CA9 days ago
$90,000–$140,000 Per Year
Guided by the core values of Beautiful, Healthy, and Refreshing, they innovate beyond traditional cosmetics and household products, delivering creative solutions tailored to evolving consumer needs. As the Senior Regulatory Affairs Manager, you will ensure regulatory compliance for cosmetic, OTC, dietary supplement, and medical device products in North America—from concept to market launch.

Los Angeles, CA9 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.

CA9 days ago
Remote
$140,000–$210,000 Per Year
The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
Participate and support as an active member of a multi-disciplinary team to establish Regulatory CMC strategies for commercial products, late- and early-stage development programs, under the supervision of GRA-CMC leadership.

Thousand Oaks, California30+ days ago
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.

Orange, CA7 days ago
$68,015–$108,824 Per Year
p>We are hoping you will join us as a Regulatory Affairs & Compliance Analyst, Policies & Procedures and help shape the future of healthcare where you'll be an integral part of our OOC - Policies & Procedures team, helping to strive for excellence while we serve our member health with dignity, respecting the value and needs of each of our members through collaboration with our providers, community partners and local stakeholders.
Bachelor's degree in health services administration, public health, public policy or related field PLUS 3 years of experience in the health care industry in a public or regulatory affairs role, including experience in policies and procedures development, required; an equivalent combination of education and experience sufficient to successfully perform the essential duties of the position such as those listed above may also be qualifying.

Orange, California30+ days ago
li>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.

Thousand Oaks, CA30+ days ago
$255,302–$345,408 Per Year
p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

New!
Brea, CA5 days ago
$85,800–$104,800 Per Year
This individual is responsible for obtaining global regulatory registrations/approvals based on company objectives, attending product development meetings, regional alignment; as well as collaborating with cross-functional departments to ensure country-specific requirements are met and integrated throughout the design control and post-product launch activities. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.

New!
Brea, California6 days ago
This individual is responsible for obtaining global regulatory registrations/approvals based on company objectives, attending product development meetings, regional alignment; as well as collaborating with cross-functional departments to ensure country-specific requirements are met and integrated throughout the design control and post-product launch activities. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.

Pasadena, CA30+ days ago
$280,000–$320,000 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.

Thousand Oaks, CA7 days ago
p>In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.

New!
Orange, California6 days ago
$26.60–$43.82 Per Hour
li>Demonstrated 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.

West Hollywood, CA26 days ago
$120,000–$145,000 Per Year
Full-time
Oversee product testing processes, including sample coordination, protocols, vendor quotes, and method validation to ensure accuracy, reliability, and regulatory compliance of testing procedures. We are seeking a highly detail-oriented QA & Regulatory Sr Manager to oversee product compliance, safety, and quality systems across the full product lifecycle.

New!
Los Angeles, CA4 days ago
$130,000–$178,000 Per Year
li>Work closely with other teams at Zoox, including Legal,
Communications, and Safety teams, to ensure up-to-date knowledge of company plans and report on policy/political developments with clear analysis. Anchored on facilitating our expansion to Los Angeles, this exciting new role will build on our positive political reputation and help guide our local operations from testing to commercial deployment.

Los Angeles, CA23 days ago
$280,000–$320,000 Per Year
div class="content-pay-transparency">
California pay range
$280,000—$320,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 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.

Thousand Oaks, California30+ days ago
Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. In this key role you will serve as the functional area lead on product teams, lead writing activities for complex product submissions, provide functional area expertise, train and mentor more junior writers, and lead departmental activities.

El Segundo, CA26 days ago
li>
Craft a modern regulatory strategy based in sound engineering principles with input from executives, our board of directors, and industry experts that brings the safest product to market the fastest. Portable nuclear power with rapid-deploy capability can replace similar-sized diesel generators and provide critical asset support for hospitals, data centers, remote sites, and military bases.

Rosemead, CA27 days ago
In this job, you'll be developing and advocating the Company's positions associated with wholesale generation and energy storage interconnections to SCE's distribution system, including managing the development of revisions to SCE's wholesale distribution access tariff.
Become a Utility Regulatory Affairs Senior Advisor at Southern California Edison (SCE) and help meet our goals of interconnecting clean energy resources to SCE's grid.

CA30+ days ago
$147,000–$184,000 Per Year
li>Provide operational and strategic input into planning for expanded access programs and study specific documents such as synopses, protocols, ICFs, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plans, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
Essential Job Functions and Responsibilities:
These may include but are not limited to:
Provide oversight of clinical affairs programs across all functional areas of the drug development process, including post-trial access programs coordinating the continued provision of investigational product to participants, in accordance with regional regulations.

Westlake Village, CA30+ days ago
p>Duties and Responsibilities:
Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA, ANVISA, ANMAT, and other relevant regulatory bodies and/or Distributors.
Provide support for clinical studies, such as preparing and/or submitting regulatory documents, interaction between sites, support site requests, technical documentation, maintenance of all study files.

New!
Santa Monica, CA5 days ago
p>Accountabilities:
Global Regulatory Leadership: Own the end-to-end global regulatory strategy for a high-complexity cell and gene therapy program, from current stage through BLA submission, ensuring an efficient route to approval with competitive labeling aligned to product attributes and patient, market and business needs.
Cross-Functional Product Leadership: Represent Regulatory Affairs on Global Product Teams, shaping development and commercialization plans, contributing to governance presentations and aligning regulatory objectives with clinical, CMC, safety and commercial strategies.

New!
Rosemead, CA2 days ago
In this job, you'll be developing and advocating the Company's positions associated with wholesale generation and energy storage interconnections to SCE's distribution system, including managing the development of revisions to SCE's wholesale distribution access tariff. Become a Utility Regulatory Affairs Senior Advisor at Southern California Edison (SCE) and help meet our goals of interconnecting clean energy resources to SCE's grid.

El Segundo, California30 days ago
li>
Craft a modern regulatory strategy based in sound engineering principles with input from executives, our board of directors, and industry experts that brings the safest product to market the fastest. . Portable nuclear power with rapid-deploy capability can replace similar-sized diesel generators and provide critical asset support for hospitals, data centers, remote sites, and military bases.

Seal Beach, California19 days ago
This executive role ensures alignment across clinical development, regulatory strategy, scientific communications, and product lifecycle management to support the successful development, approval, and commercialization of the company's products.
Develop and maintain strategic relationships with physicians, investigators, Key Opinion Leaders (KOLs), healthcare providers, and scientific experts to support clinical development, evidence generation, product adoption, and medical education initiatives.

New!
Thousand Oaks, California2 days ago
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.

CA26 days ago
$155,520–$194,400 Per Year
Cross-Functional Facilitation: Project manage non-security stakeholders to ensure the timely collection of evidence, support, and information required for successful regulatory filings and audits, working closely with the Security Compliance Regulatory Affairs team to facilitate and align on response. Scope & Response Optimization: In partnership with cyber legal counsel, define the "scope of applicability" for new regulations to ensure Twilio's responses and decisions are precise, efficient, and aligned with how we actually build products.

Los Angeles, CA30+ days ago
Visit https://adventisthealth.org/careers/everify/ for more information about E-Verify.
Licenses/Certifications:
Certified Professional in Healthcare Quality (CPHQ) or Healthcare Accreditation Certificated Professional (HACP) certification or Lean certification: Required within two years of hire.

Los Angeles, CA30+ days ago
Remote
$150,000–$170,000 Per Year
li>Serve as a scientific expert and liaison to healthcare professionals, key opinion leaders, and internal stakeholders to facilitate clinical education, evidence exchange, and trusted relationships associated with off-label inquiries, third-party validation services, health hazard assessments, etc. This role will serve as a trusted scientific partner to internal/external stakeholders-including healthcare professionals, cross‑functional teams, and external collaborators - directly influencing product adoption, appropriate use, and long‑term market success.

California, CA30+ days ago
Remote
$200,000–$230,000 Per Year
You will be responsible for bringing structure, discipline, and clear operating rhythm to a complex, multi state lobbying network, ensuring our external partners are well coordinated, accountable, and aligned to business priorities. We have an exciting opportunity to join our Government & Industry Affairs team in the United States and are currently looking for a Senior Manager, Government & Industry Affairs Operations to join the team.

CA26 days ago
Remote
p>SonicWall is seeking a highly experienced Senior Hardware Compliance Engineer to lead worldwide regulatory compliance activities for network security hardware products, including WLAN/RLAN devices and wireless access points. With the ability to build, scale and manage security across the cloud, hybrid and traditional environments in real-time, SonicWall provides relentless security against the most evasive cyberattacks across endless exposure points for increasingly remote, mobile and cloud-enabled users.

Huntington Beach, California30+ days ago
As Senior Manager, Quality Engineering, you will serve as a principal leader within the BiVACOR quality organization, responsible for architecting and directing quality engineering functions across the full product lifecycle of the Total Artificial Heart (TAH) system, one of the most technically advanced implantable devices in development today. You will not only lead the QE team in verification and validation, manufacturing process quality, supplier controls, and regulatory compliance — you will define the strategic direction of quality engineering programs, drive enterprise-level QMS maturity, and serve as a senior executive liaison across quality, engineering, manufacturing, regulatory affairs, and clinical functions.

Long Beach, CA30+ days ago
$121,000–$145,000 Per Year
p>The Hydrafacial booster portfolio is a defining commercial and clinical differentiator for SkinHealth Systems - and every booster formulation that reaches a provider's treatment room is the product of rigorous bench chemistry, stability validation, and regulatory compliance work.
An employee's pay position within the salary range will be based on several factors, including but not limited to relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs.

CA8 days ago
$102,300–$209,500 Per Year
p>Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle''s differing products, industries and lines of business. With Oracle Cerner''s innovative technology, we seamlessly package this valuable information into a range of services and solutions that integrate seamlessly into your favorite analytics tools, EHR applications like Millennium, and even new, groundbreaking applications developed in collaboration with our esteemed partners.

CA30+ days ago
$120,100–$150,100 Per Year
You will be acting as a full-stack PM, leading a cross-functional team in conducting user interviews, uncovering user pain points, gathering requirements, writing BRD/PRDs, creating user stories, defining acceptance criteria, and leading the scale of our Provider Portal for Japan. The Senior Product Manager for Oncology Provider Solutions, Japan, will own the scale of our key product lines in the Japanese market and will join a growing team that shares the critical role of being the voice of our many internal and external users.

Los Angeles, CA30+ days ago
Remote
$140,000–$170,000 Per Year
p>Ensures all clinical trials are executed in compliance with international GCP guidelines/regulations and applicable SOPs: participates in the planning of quality assurance activities and coordinates resolution of audit findings and CAPAs; ensures audit-ready condition of clinical trial documentation including the TMF; reviews monitoring visit reports to ensure quality and resolution of site-related issues; coordinates and assists in the planning of regulatory or ethics committee activities, as appropriate; participates in site monitoring visits, as appropriate.
The Senior Clinical Trial Manager (Senior CTM) is responsible for the successful execution of clinical trials from the protocol concept through the clinical study report, ensures completion of study deliverables, typically works on studies with moderate to high complexity (in terms of design, location, phase, etc.), proactively identifies and resolves clinical project issues, and participates in process improvement initiatives as required.

Santa Monica, California20 days ago
Our growing portfolio spans PMS & hormone balance, vaginal & urinary health, digestion, menopause, and conception support—offering vitamins, supplements, and personal care products that women trust. Since launching in 2018, O Positiv has reshaped the women’s health space, tackling long-overlooked issues with innovative, science-backed products and boldly breaking taboos along the way.

West Hills, CA11 days ago
$117,000–$195,000 Per Year
li>Excellent communication skills which foster the ability to lead through influence, living a culture of quality, accountability, and continuous improvement while guiding teams toward sound, risk-based decisions without direct authority.
The Manager, Design Quality reports directly to the Director of Design Quality and works closely with cross-functional teams across Pharmavite.

El Segundo, CA30+ days ago
This role will support GMP production activities, both internally at ImmunityBio and at external parters or CMOs (Contract Manufacturing Organizations), for both clinical and commercial products by developing and implementing quality control processes, analyzing data to identify issues, collaborating with cross-functional teams, and driving continuous improvement initiatives to maintain phase appropriate compliance to regulations.
Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.

Long Beach, California30+ days ago
The Hydrafacial booster portfolio is a defining commercial and clinical differentiator for SkinHealth Systems — and every booster formulation that reaches a provider's treatment room is the product of rigorous bench chemistry, stability validation, and regulatory compliance work. An employee’s pay position within the salary range will be based on several factors, including but not limited to relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs.

Seal Beach, California7 days ago
p style="margin:0px">The Associate Director/Manager, Field Medical Affairs is a key member of Dendreon’s Medical Affairs leadership team and serves as a player-coach, providing national leadership for the U.S. Medical Science Liaison (MSL) team while maintaining direct field responsibilities across the Western United States (WA, AK, OR, ID, MT, WY, CO, ND, SD, NE, KS, CA, NV, UT, AZ, NM).
Minimum 3 years of experience as an MSL, including 1+ years in an established leadership capacity (team lead, regional MSL manager, or direct people management).

West Hills, CA30+ days ago
$113,500–$170,200 Per Year
p>This is primarily a product operations and execution leadership role, responsible for driving product lifecycle execution including launch readiness, design transfer, lifecycle changes, and obsolescence while ensuring alignment with regulatory and quality requirements.
Lead and develop team members, including Associate Product Managers responsible for lower-complexity and mature products, ensuring execution within established portfolio strategy and decision-making guardrails.

West Hills, California21 days ago
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For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards.

Los Angeles, CA23 days ago
$190,000–$260,000 Per Year
div class="content-conclusion">
ITAR Compliance:
To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR here.

New!
Santa Clarita, CAToday
$100,320–$125,400 Per Year
strong>A minimum of 200Mb/sec download and 10Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova. Advanced Bionics is seeking a Senior Specialist, International Regulatory Affairs to support global regulatory activities for Class III medical devices.

Whittier, CA27 days ago
$102,481.60–$169,104
Full-time
The fully integrated network is comprised of PIH Health Downey Hospital, PIH Health Good Samaritan Hospital, PIH Health Whittier Hospital, 37 outpatient medical office buildings, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, digestive health, orthopedics, women’s health, urgent care and emergency services. The Project Manager collaborates with cross-functional teams including Regulatory Affairs, Supply Chain, Contracts, Finance, Governance, FF&E, Clinical Operations, and Information Technology, applying AEC Best Practices and PMI-aligned methodologies to deliver safe, efficient, and future-ready environments for patient care.

Costa Mesa, CA30+ days ago
The role partners closely with Product Development, Sourcing, Quality, and Legal teams to support compliance efforts related to product safety, chemical and material restrictions, supply chain transparency, labeling, and extended producer responsibility (EPR). Additionally, employees can choose from several voluntary benefits including: Hospital Indemnity/Accident insurance; Flexible Spending Account/Health Saving Account; Employee Assistance Program; Paid Time Off/Paid Holidays/Sick Time; Casual Dress Code; and Employee Discounts.

Valencia, CA7 days ago
$100,320–$125,400 Per Year
p>Advanced Bionics is seeking a Senior Specialist, International Regulatory Affairs to support global regulatory activities for Class III medical devices.
Responsibilities:
Plan and execute global regulatory activities to obtain and maintain approvals in international markets, including LATAM, EMEA, and APAC.

CA16 days ago
Remote
We offer an expanding suite of products - from fully-digital embedded renters coverage to high-value homeowners insurance to sophisticated commercial coverages, such as cyber liability and habitational property - delivered through agents, brokers, wholesalers and other brand partners.
Own and drive the rate and rule revision process end-to-end: confirming scope and timelines, preparing regulatory filings, coordinating with vendors, responding to regulator inquiries, and implementing approved changes.

Los Angeles, CA30+ days ago
$107,000–$133,000 Per Year
The AC has a four-part mission to: (a) advance and support clinical trials and therapeutic development for cell and gene therapies; (b) engage diverse and underserved communities in those trials and the resulting therapies; (c) provide training and education to r searchers, staff, patients, and communities; and (d) exchange expertise with other AC network sites and community partners. The University of Southern California (USC) is actively seeking a full-time Clinical Operations Senior Project Manager for the USC+CHLA Alpha Clinic (AC), a pre-clinical/clinical infrastructure program serving USC and Children's Hospital Los Angeles (CHLA).

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Regulatory Manager Jobs in Beverly Hills, CA

Regulatory Affairs & Quality Assurance Manager University of California, Irvine

Bilingual Korean/English Senior Regulatory Affairs Manager - Cosmetics, OTC & Supplements (FDA Compliance Macpower Digital Assets Edge Private Limited

Quality Systems & Regulatory Manager Jobot

Senior Manager, Global Regulatory Affairs, CMC Jazz Pharmaceuticals Plc

Regulatory Affairs, Sr Manager – Obesity and Related Conditions Amgen

Regulatory Affairs & Compliance Analyst, Policies & Procedures CalOptima

Regulatory Affairs Coordinator University of California, Irvine

Executive Director of Regulatory Affairs - Obesity and Related Conditions Amgen Inc

Regulatory Affairs Specialist II Envista Holdings Corp

Regulatory Affairs Specialist II Envista Dentistry

Executive Director, Regulatory Affairs Arrowhead Pharmaceuticals Inc

Regulatory Affairs Sr Manager, Regulatory Promotion & Material Compliance Amgen Inc

Assistant Regulatory Affairs Coordinator University of California, Irvine

Sr Manager of Quality & Regulatory Michael Page USA

Government Affairs and Public Policy Manager, Cities Zoox Inc

Executive Director, Regulatory Affairs Arrowhead Pharmaceuticals

Regulatory Writing Sr Mgr Amgen

Director of Regulatory Affairs Radiant Industries Inc

Utility Regulatory Affairs Senior Advisor Edison International

Senior Medical Affairs Operations Manager Crinetics Pharmaceuticals Inc

Sr. Regulatory Affairs Specialist Caldera Medical Inc

Executive Director, Regulatory Affairs Strategy - Cell and Gene Therapy AstraZeneca Plc

Utility Regulatory Affairs Senior Advisor Southern California Edison

Director of Regulatory Affairs Radiant Industries

Vice President, Regulatory Affairs, Clinical Operations & Medical Affairs Dendreon Corporation

U.S. Regulatory Strategy – Obesity and Related Conditions, Senior Manager Amgen

Senior Security Regulatory Compliance Manager Twilio Inc

Program Manager, Accreditation and Regulatory Compliance (White Memorial) Adventist Health System

Manager, Clinical Science, Medical Affairs Danaher Corp

Senior Manager, Government & Industry Affairs Operations VGW Holdings Ltd

Regulatory Manager SonicWALL Inc

Senior Manager, Quality Engineering BiVACOR

Senior Manager, Formulation Development Beauty Health Group Limited

Principal Product Manager Oracle Corp

Sr Product Manager, Oncology Japan Natera Inc

Senior Clinical Trial Manager - Remote Position Puma Biotechnology Inc

Research & Development Manager O Positiv

Manager, Design Quality Pharmavite LLC

Value Stream Quality Manager ImmunityBio Inc

Senior Manager, Formulation Development BeautyHealth

Associate Director/Manager, Field Medical Affairs Dendreon Corporation

Manager, Product Operations (Transplant Diagnostics) - West Hill, CA Thermo Fisher Scientific Inc

Manager, Product Operations (Transplant Diagnostics) - West Hills, CA Thermo Fisher Scientific

Director of Regulatory Inversion

Senior Specialist, International Regulatory Affairs (Valencia (CA), United States) Sonova AG

Project Manager, Facilities Construction - FT Days PIH Health

Product Compliance Manager 5.11 ABR Corp

Senior Specialist, International Regulatory Affairs Sonova Holding AG

Senior Product Manager, Homeowners - MSI The Baldwin Group Insurance Holdings, LLC

Clinical Operations Senior Project Manager University of Southern California

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