134 Results for

Regulatory Manager Jobs in Irvine, CA

Jobs

Lake Forest, CA

The Manager I, Regulatory Affairs Strategy (Professional Path) ), reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory affairs activities, including product submissions, renewals, and updates, while ensuring compliance and competitive advantage.

Collect and analyze regulatory intelligence for China to ensure product compliance and engage in industry associations like Advanced Medical Technology Association (AdvaMed) and Asia Pacific Medical Technology Association (APACMed).

10 days ago

Lake Forest, CA

Manager, Regulatory Affairs Strategy (Professional Path), reporting to the Senior Director of Regulatory Affairs (LLSI), is primarily responsible for setting or executing the regulatory strategy, leading and managing, acting as a strategist, ensuring local product registration and facilitating health registration approvals, and supporting the Senior Director during due diligence and integration activities for Business Development & Licensing projects.

In this role, a typical day will include:

A self-starter, assertive leader who will be accountable for the End-to-End regulatory support for the anterior/posterior ophthalmologic products including, but not limited to, new products, sustaining legacy products, and improvements to the product lines.

10 days ago

$105,000–$175,000 / year

You will support regulatory strategy execution with a focus on medical device consumables and accessories within the Surgical franchise, partnering cross‑functionally to ensure alignment with evolving regulatory expectations. Our benefits program provides security for life events through life and disability insurance, supports savings for retirement, promotes good health and well-being and supports associates and their families during times of illness.

30+ days ago

Lake Forest, California

p style="text-align:inherit"/>

Find Jobs for Contingent Worker. The Manager I, Regulatory Affairs Strategy (Professional Path) ), reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory affairs activities, including product submissions, renewals, and updates, while ensuring compliance and competitive advantage.

11 days ago

Irvine, California

Remote

For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.

Assist in performing and managing the initial part of the workflow (Initial QC, routing, scheduling meetings, etc.) in the Veeva system for material review and approval of the materials submitted from the assigned business units.

19 days ago

Lake Forest, California

Find Jobs for Contingent Worker.

11 days ago

Orange, California

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.

30+ days ago

CA
p>If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
25 days ago

Irvine, CA
li>Oversees the operations productivity and development of assigned regulatory staff that are responsible for ensuring that advertising and promotion materials are accurate, competitive and compliant with internal policies, Code of Federal Regulations (CFR), FDA guidance documents, PhRMA Guiding Principles, and the Federal Food, Drug, and Cosmetic Act.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html.
18 days ago

Irvine, CA
p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
13 days ago

Irvine, CA
$145,000–$205,000 / 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.
30+ days ago

Irvine, CA
Remote
$120,000–$168,000 / year
Let's talk about some of the key responsibilities of the role: Assist in performing and managing the initial part of the workflow (Initial QC, routing, scheduling meetings, etc.) in the Veeva system for material review and approval of the materials submitted from the assigned business units. A Few Other Details Worth Mentioning: The position can be either Remote or based in our beautiful Irvine office, complete with onsite gym, pool, snacks, drinks, and occasional catered meals.
30+ days ago

Irvine, CA
li>Represents Device Regulatory Affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
30+ days ago

Foothill Ranch, California
This role oversees regulatory strategy, product compliance, hazard communication, and chemical risk management to ensure adherence to applicable local, regional, and international regulations. The position partners cross-functionally with R&D, Quality, Supply Chain, and Manufacturing to support product development, market access, and ongoing regulatory compliance.
12 days ago

Orange County, CA
Remote
$127,000–$165,000 / year
For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121.
Lead FDA submissions (510(k) or pre-submissions) with the team, including wearable devices, as well as artificial intelligence (AI) Software as a Medical Device (SaMD) products.
30+ days ago

Foothill Ranch, CA
$105,000–$120,000 / year
Part time
This role oversees regulatory strategy, product compliance, hazard communication, and chemical risk management to ensure adherence to applicable local, regional, and international regulations. The position partners cross-functionally with R&D, Quality, Supply Chain, and Manufacturing to support product development, market access, and ongoing regulatory compliance.
12 days ago

CA
Remote
$140,000–$210,000 / 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.
8 days ago

Irvine, CA
li>Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations Product Teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions and stays abreast of regulatory procedures and changes in the external regulatory environment.
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html.
30+ days ago

Irvine, CA
div> Responsibilities:
In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets such as USA (FDA), EU (MDR), China (NMPA), and more.
You will work cross-functionally with Clinical, Global Regulatory Affairs counterparts, and others to support innovation and expand market access for our advanced ultrasound technologies and solutions.
30+ days ago

Lake Forest, CA
Associate, Regulatory Affairs Strategy (Professional Path) , reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory compliance for Alcon's product portfolio, managing local initiatives, and supporting business requests for product and regulatory information.
Data requests to R&D for tender applications, one-off requests for country-specific technical information, maintenance of project status master slide deck for regional RA calls, drafting (not signing) explanation letters, and other administrative requirements for HA queries.
10 days ago

New
Orange, CA
$68,015–$108,824 / 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.
6 days ago

Lake Forest, California
Associate, Regulatory Affairs Strategy (Professional Path) , reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory compliance for Alcon's product portfolio, managing local initiatives, and supporting business requests for product and regulatory information.
Find Jobs for Contingent Worker.
11 days ago

Tustin, CA
$99,498–$151,719 / year
Requires a minimum of 6 years' experience in aerospace or similar industry having technical regulatory requirements with a bachelor's degree in an engineering or technical discipline (STEM required); or 4 years of experience with a Master's Degree; and a minimum of 4 or more years of management and/or leadership experience. We are seeking an experienced aerospace Engineering Manager, FAA Regulatory Compliance to lead the critical activities that ensure regulatory compliance related to our vehicles and mission operations.
30+ days ago

New
Brea, CA
$85,800–$104,800 / 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.
4 days ago

Orange, California
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.

30+ days ago

Irvine, CA
With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications. Responsibilities: Manages medium to high impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.
18 days ago

New
Brea, California
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.
Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs.
5 days ago

Aliso Viejo, CA
p>Industry Surveillance:
Monitors competitive claims, FDA's and FTC''s actions, litigation, news releases and other sources, as they relate to the current science of Metagenics-related products and challenges to relevant product claims, to ensure that Metagenics limits its exposure for product claims both domestically and internationally.
The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.
27 days ago

Pomona, CA
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.
30+ days ago

Rosemead, CA
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.
26 days ago

New
Orange, California
$26.60–$43.82 / 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.

5 days ago

Irvine, CA
2025 University of California, Irvine, UCI Health, and UC Regents. Sign-up to be notified of hiring events, newly posted job opportunities, and much more.
19 days ago

Irvine, CA
p>2025 University of California, Irvine, UCI Health, and UC Regents.
Sign-up to be notified of hiring events, newly posted job opportunities, and much more.
30+ days ago

Seal Beach, California
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.
18 days ago

Irvine, CA
$80,000–$100,000 / year
p>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.
Prepare regulatory submissions for new products and product changes as required to ensure timely approval for clinical studies and product market release.
30+ days ago

New
Rosemead, CA
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.
1 day ago

Irvine, CA
$80,000–$100,000 / year
p>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.
30+ days ago

California, CA
Remote
$200,000–$230,000 / 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.
30+ days ago

Irvine, CA
$140,000–$175,000 / year
The role operates at the intersection of R&D, Regulatory Affairs, and Manufacturing, driving quality planning, design assurance activities, and risk management execution across the full product development lifecycle - including post-launch monitoring and stability validation through commercial steady state. Manager, New Product Quality leads and develops a team of New Product Quality Engineers responsible for ensuring the quality and regulatory compliance of medical device products from early-stage design through commercial launch and launch stability.
30+ days ago

Irvine, CA
p>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.
30+ days ago

Huntington Beach, California
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.
30+ days ago

Long Beach, CA
$121,000–$145,000 / 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.
30+ days ago

San Juan Capistrano, CA
$125,000–$145,000 / year
Responsibilities: Lead, develop, and direct a team of quality engineers or equivalent personnel supporting receiving inspection, acceptance activities, process validation, change control, supplier quality interfaces, investigations, and CAPA executionCreate an operating environment that is disciplined execution, responsive, and audit ready. Excellent cross-functional collaboration skillsStrong communication skills for effective interaction with internal teams' suppliers, and regulatory bodies61026Quest Diagnostics honors our service members and encourages veterans to apply.
28 days ago

Irvine, CA
p>The Senior Manager, Quality Assurance Compliance serves as a key Quality leader at the Irvine Technology Center (ITC), responsible for strengthening the site's quality systems, compliance posture, and audit readiness.
Serve as Deputy PRRC for ITC, supporting PRRC responsibilities under EU MDR, including oversight of quality system effectiveness, compliance-related activities, and escalation of regulatory risks as appropriate.
30+ days ago

Long Beach, California
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.
30+ days ago

Irvine, CA
Manager is responsible for partnering with leaders in Commercial, Regulatory, Medical, Legal, Compliance, BTS and other functions to ensure an efficient & compliant marketing operation function supporting Allergan Aesthetics business needs. Works closely with Brand Marketing, the PRC Committee, Compliance, and the rest of Marketing Operations, to proactively identify and resolve issues and ensure reviews are efficiently completed throughout various stages of the process.
13 days ago

New
Seal Beach, California
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).
6 days ago

Irvine, CA
In this role, you will develop strong scientific and technical product knowledge and serve as a key resource to country Regulatory Affairs associates by providing regulatory guidance and information. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
30+ days ago

Rancho Santa Margarita, CA
$71,000–$80,000 / year
The Associate Labeling Specialist works cross-functionally to support labeling projects from design input through final approval, making this an ideal opportunity for professionals with a background in regulatory affairs, quality assurance, or technical writing in the medical device industry. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.
30+ days ago

Stand out to leading employers.

Upload your resume and let employers find you for new Regulatory Manager job openings. Plus, receive relevant job matches delivered straight to your inbox.

Create A Free Account

Regulatory Manager Jobs in Irvine, CA

Regulatory Affairs Manager I Alcon Inc

Senior Manager, Regulatory Affairs Strategy Alcon Inc

Manager II, Regulatory Affairs Strategy Alcon Inc

Regulatory Affairs Manager I Alcon Research

Manager II, Regulatory Affairs the Tarsanet Internal Career Center

Senior Manager, Regulatory Affairs Strategy Alcon Research

Regulatory Affairs & Quality Assurance Manager University of California, Irvine

Regulatory Affairs Manager - Cardiovascular Surgery Medtronic Plc

Senior Manager Regulatory Affairs US Advertising and Promotion - US Specialty AbbVie Inc

Senior Manager Regulatory Affairs US Advertising and Promotion - Immunology AbbVie Inc

Senior Manager, Regulatory Affairs TMTT Edwards Lifesciences

Manager II, Regulatory Affairs Tarsus Pharmaceuticals Inc

Manager Regulatory Affairs Device-Combination Products AbbVie Inc

CMS Chemical Regulatory Manager RED Digital Cinema

Manager, Regulatory Affairs iRhythm Holdings Inc

CMS Chemical Regulatory Manager Red Digital Cinema, Inc.

Senior Manager, Global Regulatory Affairs, CMC Jazz Pharmaceuticals Plc

Manager Regulatory Affairs-Chemistry Manufacturing & Controls CMC AbbVie Inc

Regulatory Affairs Manager Katalyst Healthcares & Life Sciences

Senior Regulatory Affairs Associate Alcon Inc

Regulatory Affairs Manager Karwell Technologies

Regulatory Affairs & Compliance Analyst, Policies & Procedures CalOptima

Senior Regulatory Affairs Associate Alcon Research

Engineering Manager, FAA Regulatory Compliance Virgin Galactic Holdings Inc

Regulatory Affairs Specialist II Envista Holdings Corp

Regulatory Affairs Coordinator University of California, Irvine

Senior Associate Regulatory Affairs Submission Management AbbVie Inc

Regulatory Affairs Specialist II Envista Dentistry

Sr. Specialist, Regulatory Affairs Metagenics LLC

Manager, Regulatory V 26-00077 Alura Workforce Solutions

Utility Regulatory Affairs Senior Advisor Edison International

Assistant Regulatory Affairs Coordinator University of California, Irvine

Sr. Program Manager Regulatory Affairs - Risk Management - FT Days University of California

Regulatory Affairs & Quality Assurance Manager University of California

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

Regulatory Affairs Specialist Nihon Kohden

Utility Regulatory Affairs Senior Advisor Southern California Edison

Regulatory Affairs Specialist Nihon Kohden Corp

Senior Manager, Government & Industry Affairs Operations VGW Holdings Ltd

Sr Manager, NPI Quality Engineering Masimo Corp

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

Senior Manager, Quality Engineering BiVACOR

Senior Manager, Formulation Development Beauty Health Group Limited

Manager, Quality Operations (CDx/GMP) Quest Diagnostics Inc

Sr. Manager, Quality Assurance Compliance Alcon Inc

Senior Manager, Formulation Development BeautyHealth

Senior Manager Marketing Operations- Allergan Aesthetics AbbVie Inc

Associate Director/Manager, Field Medical Affairs Dendreon Corporation

Sr. Associate II, Regulatory Affairs Strategy Alcon Inc

Associate Labeling Specialist - Regulatory Affairs Applied Medical Resources Corp

Similar Job Searches