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Brief team/department description: As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Manager will be responsible for overseeing and managing the regulatory activities for assigned products/projects and will serve as the regulatory representative on cross-functional teams for assigned projects. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.

Azurity Pharmaceuticals Inc

Senior Manager, Regulatory Affairs

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Apply solid working knowledge of drug, biologic, and device development processes, laws, regulations, and guidelines from the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Pharmaceuticals and Medical Devices Agency (PMDA), and International Council for Harmonization (ICH). Demonstrate understanding of major regional and global industry association priorities, such as those of the Pharmaceutical Research and Manufacturers of America (PhRMA), the European Federation of Pharmaceutical Industries and Associations (EFPIA), and the Japan Pharmaceutical Manufacturers Association (JPMA).

Parexel

Senior Regulatory Affairs Associate - Regulatory Intelligence

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With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. This position collaborates with cross-functional teams to provide regulatory input during product development and throughout the product lifecycle, helping to secure timely product approvals and regulatory clearances.

CorDx

Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)

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Regulatory Affairs Manager (Atlanta)

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In our more than 1,300 community branches and across the U.S., team members help millions of customers solve critical financial needs, including debt consolidation, home and auto repairs, medical procedures and extending household budgets. You can steer your career toward leadership roles such as Branch Manager and District Manager by taking advantage of a variety of robust training programs and opportunities to advance.

HOUR

For over 100 years, we’ve been helping hard-working people tackle life’s challenges by providing the help you need when you need it. Our loan experts are from your community, understand your unique situation, and will treat you with honesty, dignity, and respect. Our goal is to deliver the best customer experience and empower you to take control of your finances.

OneMain Financial

Loan Sales Specialist

TMP PX

Working in close collaboration with Product Developers and cross-functional specialists in Food Safety, Quality, Regulatory, Nutrition, and Manufacturing, you will support sound formulation decisions, facilitate alignment across stakeholders, and guide validation and corrective actions. POSITION SUMMARY As a Senior Recipe Formulation Specialist, your mission is to drive the product recipe lifecycle from new product brief to launch, ensuring compliant formulation, effective recipe management and ingredient specification excellence.

Nestle SA

Senior Recipe Formulation Specialist

The Associate Director/Director partners closely with executive leadership to guide portfolio and business-critical decisions, supports the company by preparing materials and presentations required for high-level interactions with health authorities, and develops the next generation of regulatory leaders. This role reports to the Vice President, Head of Regulatory and is accountable for driving regulatory strategy across all portfolios-with a focus on diagnostics and device commercialization-influencing external regulatory policy, and ensuring global compliance in alignment with corporate objectives.

YEAR

Grail Inc

Associate Director, Global Regulatory Affairs # 4809

The Quality Systems Specialist II leads the coordination and preparation of document packages for internal audits, FDA inspections and external audits, and supports the Quality Director and Regulatory Affairs with quality system content for regulatory submissions. Leads preparation for, and serves as a front-room or back-room representative during, FDA inspections and external audits, including coordinating document requests, drafting responses to observations, and managing associated corrective actions, in compliance with established procedures and work instructions.

Elucent Medical Inc

Quality Systems Specialist II

Licensing Requirements: Valid driver’s license Michigan CDL Class B, or the ability to obtain within six (6) months of hire Important Compliance Requirement: This position requires obtaining and maintaining a CDL and is therefore subject to FMCSA and U.S. DOT regulations, including drug and alcohol testing. Role Summary: Please note: after training is completed, this position will work 1pm to 9:00pm Maintain an effective and organized inventory system for Fleet Services including; machines, equipment, parts, tools, supplies, fuel and services for operation.

City of Ann Arbor

Fleet Parts Specialist

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The role serves as a critical interface between Medical Affairs and global R&D, Early/Clinical Development, Global Product Development and Commercialization functions, to ensure regional insights and priorities are understood, communicated, and appropriately considered within the Global Product Team (GPT), Commercial Development Team (CDT), Medical Functional Matrix Team (FMT), and governance forums including the Portfolio Governance Committee (PGC) and Development Project Review Committee (DPRC). Contribute Medical Affairs expertise to inform early development activities for early pipeline assets, including Target Product Profile (TPP) development, clinical trial design and lifecycle planning based on regional insights and aligned future therapeutic landscape scenarios.

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing, and commercializing meaningful products that address unmet medical needs.
We have a diverse portfolio of products and product candidates, with a focus in the areas of sleep and hematology/oncology. We also support commercial products in other therapeutic areas where we can meaningfully address serious medical needs.
As part of our unwavering commitment to improve patients’ lives, we are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. We do this through a growth strategy of growing sales of the existing medicines in our portfolio; acquiring commercial products or product candidates that are in late-stage development; and pursuing focused development of our pipeline of differentiated therapies.

Jazz Pharmaceuticals

Senior Director, Global Medical Director, Neuro-Oncology

As the US #1 Veterinarian recommended pet food brand, knowledge is our first ingredient with 220+ veterinarians, PhD nutritionists and food scientists working to develop breakthrough innovations in pet health. Our journey begins with our people-developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging.

The small soap and candle business that William Colgate began in New York City early in the 19th century is now, more than 200 years later, a truly global company serving hundreds of millions of consumers worldwide. Throughout this history, Colgate people and Colgate values have been at the heart of our success.
Today, Colgate focuses on four core businesses Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate now sells its products in over 200 countries and territories worldwide.

Colgate-Palmolive Co

Business Affairs & Content Rights Specialist

Position Purpose: The Director, Global Regulatory Strategy will be responsible for developing and delivering global regulatory strategies to ensure products are developed, approved, and maintained in compliance with health authority requirements and in alignment with the corporate strategy for Stoke's portfolio. Develops and maintains current regulatory knowledge and provides guidance to regulatory staff and company management; identifies the need for new or expanded regulatory policies, processes and SOPs, and approves and ensures implementation to establish a compliant culture.

Stoke Therapeutics Inc

Director, Global Regulatory Affairs

This role is ideal for a senior regulatory professional who understands how to navigate complex agency requirements, prepare and review high-quality permit documents, evaluate project risk, and serve as a trusted technical resource for project teams, clients, and regulatory partners. The Regulatory Specialist IV will lead and support environmental permitting efforts across multiple project phases, from early feasibility and proposal support through project development, agency coordination, implementation, compliance, and closeout.

Resource Environmental Solutions LLC

Regulatory Specialist IV

While performing the essential job functions of this position, the employee is regularly required to sit, stand, talk, hear, walk, use hands and fingers, handle or feel objects, and reach with hands and arms. Peoples Security Bank & Trust Company is seeking a Loan Servicing Specialist to support the full lifecycle of our commercial, consumer, and real estate loan portfolios.

Peoples Security Bank & Trust Company

Loan Servicing Specialist I

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INNOV2026 #Hiring #IRACompliance #ComplianceAdministrator #PrevailingWage #DavisBacon #CertifiedPayroll #LCPtracker #ApprenticeshipCompliance #ConstructionCompliance #ConstructionJobs #EngineeringJobs #CleanEnergy #InflationReductionAct #IRAJobs #ProjectCompliance #LaborCompliance #PayrollCompliance #HRJobs #ConstructionManagement #EPCJobs #TexasJobs #JobOpening #CareerOpportunity #NowHiring #Recruitment. With the increasing importance of Inflation Reduction Act (IRA) requirements for clean energy construction projects, the organization is seeking an experienced Payroll Compliance Specialist to support prevailing wage and registered apprenticeship compliance.

Founded by CPA firms in 1994, Creative Financial Staffing has spent over 30 years helping job seekers and employers succeed. In fall 2025, we rebranded as CFS—a name that reflects our full range of expertise while staying true to the trusted company you know.CFS is the industry’s leading employee-owned staffing firm, connecting top talent in accounting, finance, technology, and human resources. We provide skilled professionals on both a temporary and permanent basis across diverse industries, leveraging our extensive network to match the right people with the right opportunities.Our dedication to excellence extends to our award-winning culture, recognized repeatedly for growth, recruiting, workplace environment, and employee support. Honors include Forbes’ “America’s Best Recruiting and Temporary Staffing Firms,” Staffing Industry Analysts’ top U.S. staffing rankings, FlexJobs’ Top 100 Companies for Remote and Hybrid Work, Top Workplaces USA, Newsweek’s Best Practices awards, and more.

Payroll Compliance Specialist

Leoforce - Creative Financial Staffing

Broad accounting exposure across GL, month-end close, audits, tax, revenue recognition, leases, and fixed assets. The role offers excellent exposure across the accounting function, along with outstanding benefits, generous PTO, and flexible work hour s.

Senior Accounting Specialist

HSA/FSA: Health savings and flexible spending account options with pre-tax contributions; Employee support: Employee assistance resources for employees and eligible family members; Optional coverage: Supplemental life, accident, critical illness, hospital indemnity, and whole life insurance options; Life and disability: Employer-paid basic life and AD&D insurance, plus short- and long-term disability coverage. By delivering guidance, training, and practical support, you strengthen quality and regulatory awareness across local teams and contribute to KPI reporting, process improvements, complaint handling, post-market surveillance, and service-calibration activities where applicable.

Eppendorf

Quality & Regulatory Affairs Specialist

Accepts responsibility to quickly identify any areas that lack cohesiveness, bringing them to the attention of leadership and working with the team in a supportive manner to resolve issues and actively look for ways, and reinforce actions needed, to achieve synergy possible within the larger organization. quality, security, office environment, company policies, continuous improvement); understands the responsibility to maintain familiarity with the systems and this position's role in support of these systems - including a consideration of the impact of individual actions on the systems and the responsibility to communicate concerns and improvement ideas.

Simmons Prepared Foods

Product & Regulatory Specialist 1

Work with internal Regulatory Affairs, Quality Assurance, Technical Operations, Supply Chain and labeling teams, as well as CDMOs and other external partners, to obtain required technical documentation, resolve information gaps, align filing and implementation plans, and support continuity of supply. Prepare, review and coordinate CMC submissions and maintenance activities arising from changes, including Canadian Level III notifications and relevant DEL or labeling updates, and U.S. Annual Reports and CBE-0/CBE-30 submissions, as applicable.

Medexus Pharmaceuticals Inc

Senior Specialist, Regulatory CMC

At Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval.

Regulatory Specialist Jobs in the United States

Senior Manager, Regulatory Affairs Azurity Pharmaceuticals Inc

Senior Regulatory Affairs Associate - Regulatory Intelligence Parexel

Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking) CorDx

Regulatory Affairs Manager (Atlanta) CorDx

Loan Sales Specialist OneMain Financial

Senior Recipe Formulation Specialist Nestle SA

Associate Director, Global Regulatory Affairs # 4809 Grail Inc

Quality Systems Specialist II Elucent Medical Inc

Fleet Parts Specialist City of Ann Arbor

Senior Director, Global Medical Director, Neuro-Oncology Jazz Pharmaceuticals

Business Affairs & Content Rights Specialist Colgate-Palmolive Co

Director, Global Regulatory Affairs Stoke Therapeutics Inc

Regulatory Specialist IV Resource Environmental Solutions LLC

Loan Servicing Specialist I Peoples Security Bank & Trust Company

Payroll Compliance Specialist CFS

Senior Accounting Specialist CFS

Quality & Regulatory Affairs Specialist Eppendorf

Product & Regulatory Specialist 1 Simmons Prepared Foods

Senior Specialist, Regulatory CMC Medexus Pharmaceuticals Inc

Regulatory Compliance Specialist - Transplant Center Houston Methodist Hospital

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