compliance

3E is a company that specializes in chemical and workplace safety solutions. They provide a range of services including chemical inventory management, SDS authoring, regulatory compliance tools, and product stewardship. Their focus is on helping organizations meet compliance standards, maintain safety, and enhance sustainability in their operations, particularly in industries dealing with chemicals and materials.

Delivering intelligent compliance solutions that empower companies to reduce risk, drive continuous improvement, and create new growth opportunities. For over 30 years, 3E has provided clients with the expertise, content, live 24-7-365 environmental health and safety (EHS) support and award winning solutions required to increase chemical and workplace safety, improve product safety and stewardship, strengthen supply chain stewardship, and optimize research and development decision support.

We are deeply committed to serving our more than 5,000 customers worldwide, including nine of the world’s top ten chemical manufacturers, eight of the world’s top ten retailers, and seven of the world’s top ten pharmaceutical companies. Global locations include our corporate headquarters in Carlsbad, California, along with offices in Beijing, China; Bethesda, Maryland; Canton, Ohio; Copenhagen, Denmark; Frankfurt, Germany; Markdorf, Germany; Montreal, Quebec; Siegen, Germany; Sofia, Bulgaria; and Tokyo, Japan. 

Visit us at www.3Eco.com.

• Research and interpret global chemical regulations, including frameworks such as REACH (EU), TSCA (US), K-REACH (South Korea), GHS, and Japanese chemical control laws
• Analyze how regulatory requirements impact 3E products and translate them into structured logic for Safety Data Sheet (SDS) outputs and broader compliance solutions
• Support the development and maintenance of regulatory content pipelines across multiple products
• Draft and validate regulatory logic in collaboration with senior team members
• Monitor global regulatory updates and contribute to internal tracking, alerts, and summaries
• Provide regional expertise in Japanese regulations, ensuring accurate interpretation and relevance of content, including leveraging language and cultural understanding
• Contribute to regulatory insights related to Japan, including engagement with industry groups or associations where applicable
• Collaborate cross-functionally with regulatory specialists, product teams, Insights, and Solutions Architects
• Contribute to AI-enabled workflows by helping train and refine digital agents used for regulatory monitoring, summarization, translation, and data classification
• Identify inconsistencies or gaps in regulatory content and recommend improvements
• Participate in knowledge sharing and continuous learning across a global team

Regulatory Specialist, Chemical Regulations

Regulatory Specialist at 3E analyzing global chemical regulations and ensuring compliance. Collaborating with teams to develop regulatory solutions and contribute to AI workflows.

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

ICON plc

• Leading or significantly contributing to regulatory strategy development for clinical programmes and key milestones.
• Authoring and reviewing complex regulatory documents, including clinical trial applications, briefing documents, and major submission components.
• Interpreting global regulations, guidelines, and precedents and advising cross-functional teams on regulatory expectations and risk.
• Participating in or leading interactions with health authorities, including meeting preparation, presentation support, and follow-up.
• Providing regulatory input into clinical development plans, risk management strategies, and labelling considerations.
• Mentoring junior regulatory staff and contributing to internal standards, templates, and best practices.
• 薬事関連資料(各種面談資料、治験届等)の作成
• 当局との連携・新薬申請から承認取得までの各種対応・進捗管理
• 社内他部門との連携と薬事観点のアドバイス提供
• 薬事戦略の提案やプレゼンテーション
• 新規事業獲得にむけてクライアントへのアプローチ
• CMC関連文書作成・CMCコンサルティング全般
• 業務関連通知・規制アップデートの全体共有

Senior Regulatory Scientist

Senior Regulatory Scientist providing regulatory and scientific expertise for global clinical development at ICON. Leading strategy development, authoring documents, and mentoring staff.

Degica Co., Ltd. is a payment processing service company that offers a wide range of payment methods across various regions, including Japan, South Korea, China, Europe, and ASEAN countries. Their flagship product, KOMOJU, supports major payment methods like VISA, Mastercard, Alipay, WeChat Pay, and local options such as Konbini in Japan and Toss in South Korea. Established in 2005 and headquartered in Tokyo, Japan, Degica provides robust integrations and API documentation for seamless payment processing. The company facilitates international transactions by managing the receipt and payout of sales proceeds on behalf of their clients.

Overview
Headquartered in Tokyo, Japan, Degica is a leading provider of Japanese digital commerce solutions: our ePayment Platform Komoju provides global businesses and developers the access they need to grow and succeed in the Japanese market.

We build and manage online sales for Retail, Digital, and Gaming companies that are looking to establish and expand their business presence in Japan and South Korea.

Japan has a complex digital eco-system, with multiple payment methods and platforms often incomprehensible to outsiders. Degica offers a gateway to the market through its customizable tools and services, whether you are launching a completely new product or trying to enhance your current reach with consumers.

Company Mission
Degica is your “digital cart” in Japan. We are the link you need to connect your product or service with local customers, integrating digital payment and platforms with partners across our wide network.

Company culture
Everyone at Degica loves Japan and cares about how it interacts with the rest of the world. We believe in a borderless world, and want to play a lead role in bringing Japan to the world and the world to Japan. All of us love games and all things digital and it is in this space that we excel.

Come to see our corporate pages for more information:
www.degica.com
www.komoju.com
konbini.co.jp

Degica Co, Ltd.

• Develop, implement and maintain compliance programmes and internal policies aligned with Japanese laws & regulations in the fintech industry (e.g., Instalment Sales Act, AML/CFT, Payment Services Act, APPI).
• Manage and lead regulatory registrations, liaison with regulatory authorities, and inspections/audits (ISMS, PCI DSS, Privacy Mark, Credit Card Handling Registration, Prepaid Payment Instrument Issuer Registration, etc.).
• Act as a key compliance advisor across business units (product, operations, treasury, legal, verification, marketing, sales) to ensure compliance is efficiently built into our product design process.
• Conduct risk assessments and monitoring, oversee controls, audit readiness, internal investigations, and ensure remedial actions when needed.
• Provide semiannual compliance reports to the Board and executive team covering key areas of activity of the compliance team.
• Supervise compliance training, documentation projects, and implementation of new compliance management tools or software.
• Monitor regulatory changes, interpret their impact on the business and propose/implement changes to processes and controls.
• Manage a compliance team of 7 individuals (and growing) and ensure continuous improvement in the compliance function (mentoring, capability building).
• Collaborate with global external partners and affiliates to ensure consistent implementation of compliance standards and efficient cross-border alignment.
• Represent the company in responding to compliance due diligence requests from overseas partners, investors, and financial institutions, ensuring accurate, transparent, and timely communication.

Compliance Team Manager

Compliance Manager leading a compliance team for a rapidly growing fintech business in Tokyo. Responsible for managing compliance frameworks, regulatory engagement, and internal policies.

DuPont is a global innovation leader, focusing on essential solutions for the world, including protective equipment, clean water technologies, and advanced electronics. Known for its brands such as Kevlar®, Nomex®, and Tyvek®, DuPont delivers crucial innovations across various industries such as automotive, building and construction, and electronics. Committed to sustainability, DuPont integrates environmental considerations into its strategies and operations, aiming for net-zero emissions by 2050. With a focus on science and innovation, DuPont is set to separate into three independent companies to better address evolving market needs and drive future success.

Beware of recruitment scams! Please read important information for job seekers: https://www.dupont.com/careers/hiring-faqs.html

It's a time of incredible progress at DuPont — a time of momentum. It's the time for change makers, for the doers and pioneers, to create essential innovations the world needs. We aren’t just creating a better future, we’re working together to invent a better now. So bring your best self and join us in uncovering insights that will transform the world.

Why wait for a better future? Invent a better now. 

Learn more at dupont.com. 

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DuPont

• Responsible for supporting the continuity and growth of the business in Asia Pacific (AP) by ensuring compliance with regional regulations applicable to the company’s products and business activities.
• Execute transactional processes to ensure day-to-day regulatory compliance, such as import/export procedures related to raw materials, intermediates, and chemical/article finished products.
• Provide Product Stewardship & Regulatory (PS&R) support to both internal and external stakeholders.
• Engage in regional advocacy and contribute to the ongoing implementation and continuous improvement of product safety, hazard communication, and regulatory systems and processes.
• Participate in the screening of new raw materials as part of the Management of Change (MOC) process, and responsible for providing regulatory approvals for new products, product extensions, and product translations.
• Provide essential business information to the Chemical Management Team to support Permission, License, and Registration (PLR) processes for specific markets and applications in Asia.
• Interface with relevant local and regional business functions to define PS&R needs, based on a clear understanding of business plans—particularly those related to business development and R&D.
• Offer compliance advice and guidance to ensure effective policies and procedures are developed and maintained, and recommend strategic approaches for new product development and regulatory registrations.
• Actively participate in and support Product and Application Risk Reviews, as applicable, and ensure alignment with Product Stewardship & Regulatory Standards and Responsible Care requirements.
• Support the review and approval process for Safety Data Sheets (SDS) and product labeling.

Product Stewardship & Regulatory Consultant – m/f/d

Product Stewardship & Regulatory Consultant at DuPont ensuring compliance with product regulations in Asia Pacific. Supporting business growth through regulatory strategy and compliance management.

Takeda is a global biopharmaceutical company dedicated to bringing better health and a brighter future to patients worldwide. With a strong focus on research and development, manufacturing, and quality, Takeda operates with a commitment to ethics and a diverse workforce that spans over 80 countries. The company leverages innovative science and partnerships to create impactful medicines, including therapies in oncology and vaccines, ensuring that they effectively meet the needs of the patients they serve.

We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society.

We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities.

Read our community guidelines: https://takeda.info/communityguidelines

Takeda

• 日本における医薬品(化学合成品、バイオ医薬品)の新規申請及び承認取得後のCMC薬事に関連する下記業務に責任を持つグループの責任者
• 申請戦略・申請計画のCMCパートについて立案・遂行
• 薬事関連の当局相談に係る戦略策定及び遂行
• 製造販売承認申請業務(CMCパート)
• 導入案件のCMC薬事関連の評価
• グループメンバーの教育訓練及び人財育成

Director, Japan CMC & Devices Regulatory Affairs

Lead Japan CMC & Devices RA New Drug Application group at Takeda, overseeing regulatory strategies and team development for drug approvals. Drive communication with health authorities and stakeholder management.

Hybrid Compliance Managers roles in Japan

Browse 5 hybrid compliance managers roles hiring in Japan plus related opportunities such as risk, compliance analyst and compliance officer.

5 jobs found