Hatsudai Manulife

雇用機会

お客様は私たちにとって最も重要であり、多くのエンドユーザーは私たちの製品・サービスを信頼して安心した日々をおくることが出来ています。私たちのビジネスの将来のために、重大な問題を解決して価値を提供することが出来るJR プロダクトツール部スタッフ を求めています。あなたを必要としています。

職務詳細:

  • 商品に関する募集ツール(パンフレット/重要事項のお知らせ/契約締結前交付書面/ご契約のしおり/補助ツール等)の企画/作成
  • 商品に関する募集ツールの精査/改訂(毎年4月に実施される一斉改訂のリード含む)
  • ユニバーサル・コミュニケーション・デザイン(UCD)の推進活動

求める経験:      

  • 生命保険会社または隣接業界での実務経験2年以上
  • お客さま向けツール作成の経験があれば尚良い

スキル:

  • PCスキル(ワード/エクセル/パワーポイント)
  • 日本語(保険約款/用語を理解できる文章読解能力およびその説明資料を作成できる文章作成能力)

(人物像)

  • 周囲と良好なコミュニケーションやコラボレーションができる人

社外勤務についての部内ガイドライン:

ハイブリッド勤務になります。社外勤務は当社のガイドライン(Working Better)に従ってチームで決定いたします。

残業について:

月0~40時間

給与:

経験、能力を考慮の上、当社規定により優遇します。

通勤交通費支給(当社規定による)

変動賞与年1回(個人、会社業績に応じて支給)

勤務時間:

原則 9:00~17:00(実働7時間)

フルフレックス制度あり

福利厚生:

社会保険完備(健康保険、厚生年金保険、雇用保険、労災保)、ベネフィットワン、各種研修制度(英語、日本語研修含む)、育児・介護休業制度、ベビーシッター支援制度、wiwiwシステム(育児休業からの復職支援システム)の導入、退職金制度

休日休暇:

完全週休2日制(土・日)、祝日、年末年始、有給休暇、特別連続休暇、アニバーサリー休暇他

勤務地:

初台本社 〒 東京都新宿区西新宿三丁目20-2 東京オペラシティタワー

あなたを動機づけは何ですか?

  • あなたはお客様に一生懸命になり、お客様の利益のために耳を傾け、関与し、行動します
  • あなたはアジャイルなマインドセットでビジネスの成果を実現する方法を見つけたいという好奇心を持って、広い視野で考えます
  • あなたはチームで成長し、一緒に物事を成し遂げることを楽しみます
  • あなたは責任感をもって、重要事項に対するソリューションを構築します
  • あなたは正しいことをし、誠実に働き、率直に発言します
  • あなたの人間性を共有し、多様で包括的な職場環境を構築するのを助けます

私たちのコミットメント

  • 我々の使命; 意思決定をより簡単にし、より良い生活を送るために貢献すること
  • あなたの成長と成功のためのリーダーシップチームであること
  • 業界の変革を推進するリーダーとなるという大胆な目標
  • 毎日最善を尽くす

When you join our team:


• We'll empower you to learn and grow the career you want.


• We'll recognize and support you in a flexible environment where well-being and inclusion are

more than just words.


• As part of our global team, we'll support you in shaping the future you want to see.

jobs.manulife.comで私たちの雇用機会についてもっと学んでください

About Manulife and John Hancock

Manulife Financial Corporation is a leading international financial services provider, helping people make their decisions easier and lives better. To learn more about us, visit

Manulife is an Equal Opportunity Employer

At Manulife/John Hancock, we embrace our diversity. We strive to attract, develop and retain a workforce that is as diverse as the customers we serve and to foster an inclusive work environment that embraces the strength of cultures and individuals. We are committed to fair recruitment, retention, advancement and compensation, and we administer all of our practices and programs without discrimination on the basis of race, ancestry, place of origin, colour, ethnic origin, citizenship, religion or religious beliefs, creed, sex (including pregnancy and pregnancy-related conditions), sexual orientation, genetic characteristics, veteran status, gender identity, gender expression, age, marital status, family status, disability, or any other ground protected by applicable law.

It is our priority to remove barriers to provide equal access to employment. A Human Resources representative will work with applicants who request a reasonable accommodation during the application process. All information shared during the accommodation request process will be stored and used in a manner that is consistent with applicable laws and Manulife/John Hancock policies. To request a reasonable accommodation in the application process, contact

Working Arrangement

Hybrid

  • Hatsudai Manulife ¥30,000,000 - ¥42,000,000 per year

    We are seeking JR Product Tools Staff who can provide significant contributions to our business future by resolving major problems and delivering value. · ...


  • Shinjuku Manulife

    We are seeking a Product Tool Staff to join our team. This role involves designing and creating product-related recruitment tools such as pamphlets and notices. · The ideal candidate will have experience in the insurance industry or related fields for at least two years. They sho ...


  • Shinjuku-ku Manulife Full time

    We are looking for a JR Product Tool Department Staff who can help us solve significant problems and provide value in our business's future. · ...


  • Chūō Johnson & Johnson Innovative Medicine Full time¥1,500,000 - ¥4,000,000 per year

    +The RA staff plans regulatory affairs activities for new and existing products. · +Interpreting regulations · Leading cross‑functional implementation of compliance measures · Communicating with health authorities · +- More than 5 years of experience in regulatory affairs · - Co ...


  • 東京都 中央区, Johnson & Johnson ¥1,000,000 - ¥1,200,000 per year

    The Regulatory Affairs staff at Johnson & Johnson plans coordinates executes Regulatory Affairs activities new existing products. · Actively participate strategic discussions cross functional team members. · Plan regulatory activities assigned projects. · ...


  • Chuo-ku, Tokyo Johnson & Johnson MedTech

    The RA staff in this role plans, coordinates, and executes Regulatory Affairs activities for both new and existing products. · ...


  • 東京都 品川区 大崎, Boehringer Ingelheim

    +Job summary · The GXP Quality Assurance Specialist will oversee all aspects of quality assurance in accordance with regulatory requirements. · +ResponsibilitiesSUPervise document control defined in GQP Ordinance (SOP Quality Standard Codes) · ...


  • Shinagawa, Japan Boehringer Ingelheim

    Qualifications: Approximately 3 years of quality assurance/control area or similar business area experience. In-depth knowledge or experience of GQP/GMP/GDP. English skill (At a level where daily business activities can be ensured). Degree: Bachelor's degree(Any) · ...


  • Shinagawa, Japan Boehringer Ingelheim

    Assure proper manufacturing control and quality control in accordance with GQP/GMP/GDP regulations. · Investigate and analyze quality problems of products before shipping and take actions for improvement to manufacturers. · Apropriately manage deviation controls, change control m ...


  • Shinagawa-ku, Tokyo Boehringer Ingelheim

    Perform GXP activities according to GQP/GMP Ministerial Ordinance and GDP guideline. · SUPVISE DOCUMENT CONTROL DEFINED IN GQP ORDINANCE · ...


  • Shinagawa Boehringer Ingelheim

    We are seeking a Quality Assurance/Control Specialist to join our team at Boehringer Ingelheim Corporate. As a key member of our quality assurance team, you will play a crucial role in ensuring high-quality products reach customers safely and effectively. · You will be responsibl ...


  • Chiyoda myGwork - LGBTQ+ Business Community ¥1,800,000 - ¥2,500,000 per year

    +This role involves maintaining regulatory approvals for general surgery products including sutures and tissue adhesives. · +Promptly managing regulatory compliance activities across various regions. · Establishing strong relationships with key stakeholders within local authoriti ...


  • Chiyoda Johnson & Johnson MedTech ¥4,000,000 - ¥6,000,000 per year

    We are seeking a RegulatoryAffairs Specialist to join our team at JohnsonandJohnson.The successful candidate will be responsible for maintainingand managing regulatory approvals for pharmaceutical products including surgical suturesand adhesives. · ...


  • Chiyoda Johnson & Johnson Innovative Medicine Full time¥4,000 - ¥10,500 per year

    + · The company seeks an experienced professional for its regulatory affairs team responsible for maintaining management of Japan general surgery field products including sutures tissue adhesives etc. ...


  • Chiyoda Johnson & Johnson Innovative Medicine Full time

    We believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, · `Plan, prepare and execute necessary regulatory actions to support business objectives. · `}`Company's business strategy ...


  • 東京都 千代田区, Johnson & Johnson

    At Johnson & Johnson, · We believe health is everything. · Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,treated,and cured, · where treatments are smarter and less invasive, · and solutions are personal. · ...


  • Tokyo Manulife Full time¥3,000,000 - ¥4,500,000 per year

    We are seeking an experienced Customer Service Staff to join our team at Manulife/John Hancock. · As a Customer Service Staff, you will be responsible for creating billing data for group insurance premiums, · processing premium payments, · and improving business efficiency by pro ...


  • Tokyo Forvis Mazars in Japan ¥2,000,000 - ¥2,800,000 per year

    We are seeking an Accounting Staff~Manager to join our team in Tokyo. The successful candidate will have experience in accounting or subsidiary management at a company, and will be responsible for providing accounting advisory and coordination services to Japanese companies expan ...


  • Tokyo Rakuten

    +Job Description · 部署・サービスについて · レジャープロダクト部 (LPD) はライフスタイルやレジャーに関連するサービスを担当しており、いくつかのサービスでは日本でのトップシェアを誇っています。私たちはイノベーションとテクノロジーを通じて、グローバルな成長と世界のリーダーになることを目指しています。これを達成するため、私たちのサービス開発に貢献できるグローバルなマインドセットを持ったエンジニアを探しています。 · + · ...


  • Tokyo Rakuten

    本户 、 今复 · 星期 TPD(共호제짍는) で(😁),)세요 . · %' · ...


  • Sagamihara Johnson & Johnson MedTech ¥9,000,000 - ¥13,000,000 per year

    The RA staff plans coordinates and executes Regulatory Affairs activities for new and existing products including interpreting regulations leading cross-functional implementation of compliance measures communicating with health authorities in relation to regulatory submissions. · ...