Job Search

Every day, our consultants work with thousands of candidates to help them find the right fit for their next role. Last year, we placed over 0 candidates into permanent roles.

Our job search platform will connect you to the latest available positions across Asia.

Latest Jobs

102 listing(s) available.

  • 12 Jul 2019

    Assistant Manager, Marketing

    Singapore

    Permanent Position
    Our client is a leading MNC company with large portfolios in the consumer healthcare and OTC segments targeting to both consumers and healthcare professionals.

    Job Description

    • P & L Management
    • Development of brand  and category strategies in line with the business objectives to ensure sustainable healthy growth in Singapore and Malaysia
    • Implementation and monitoring of brand marketing plan with allocated P&L budget and meet business objectives and customer needs
    • Strategic planning and tactical action plans and execution to optimize profitability of products
    • Driving Marketing effectiveness with cluster collaboration & data driven analysis
    • Develop ATL/BTL/Digital communication plan and utilize TA insights to create customer relevant touch points and tailored trade activations to drive results effectively
    • Identify growth opportunities in trade and employed multipronged channel strategies and tactical promotions to leverage on shopper in-store behaviors & purchase patterns to drive and drive marketing effectiveness
    • Conduct in-depth business analysis and tightly monitored sales & market trends to identify gaps to bridge and potential areas of opportunities to accelerate growth
    • Work with internal (Medical, Regulatory, QA, Supply Chain) and external stakeholders to ensure proper execution of brand plans and in accordance to law and industry regulations
    Expires on 27 Oct 2019

    Posted By

    Shirley Ler Siew Yi (Reg No: R1980821)

    Tel: +65 6738 6228

    shirleyler@peoplesearch.jobs

    Requirements

    • Bachelor Degree in business or related background
    • Minimum 5 years of experience in brand management in OTC Consumer Healthcare or Beauty Industry
    • Good knowledge of the consumer market in Singapore and Malaysia
    • Strong interpersonal and communication skills

    Location : Central
    Kindly indicate your current/last salary details and your notice period

    Interested candidates kindly forward your CV to shirleyler@peoplesearch.jobs (Shirley Ler Siew Yi, Reg No: R1980821). You may email this great opportunity to someone who would be a great fit for this role.

    All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.

    PeopleSearch Pte Ltd
    EA License No: 16S8057

  • 08 Jul 2019

    Full Stack Developer

    Singapore

    Permanent Position
    In view of Digitalization, we are looking for experience Full Stack Developer for reputable Multi-national companies. To be part of the digital innovation team to drive end-to-end enterprise development. You will have an exciting opportunity to collaborate across functional teams to drive innovation and delivering application in a fast paced and vibrant environment.

    Job Description

    • As a Full Stack Developer you will also be accountable for development and maintenance of tools and processes.
    • Participate in end-to-end development process from planning to execution
    • Building high quality web apps/services by maintaining code integrity and organization.
    • Work on designs/architectures focusing on scaling the applications
    • Be constantly updated with up-to-date trends and technologies to anticipate upcoming development needs and requirements
    • Deliver know-hows that are optimized for a wide range of devices and interfaces, including mobile and web.
    • Are you a talented developer with a hunger for technology development and innovation?
    Expires on 27 Oct 2019

    Posted By

    Jasmine Tay Shi Hui (Reg No: R1875362)

    Tel: +65 6738 6228

    Jasminetay@peoplesearch.jobs

    Requirements

    • Bachelor’s degree or higher in Computer Science or related field.
    • Fluent in Microsoft technologies including Web API, .Net Core and related languages.
    • Front end development experience in HTML, CSS and JavaScript based technologies – jQuery, Angular 2+
    • Familiar with Atlassian Toolchain and APIs technologies
    • Experience in Agile Methodology
    • Experience in Open Source Development
    • Excellent verbal and written communication skills
    • Added advantage with experience in DevOps environment for CI/CD
    • 3 Positions available

    Location : Singapore
    Kindly indicate your current/last salary details and your notice period

    Interested candidates kindly forward your CV to Jasminetay@peoplesearch.jobs (Jasmine Tay Shi Hui, Reg No: R1875362). You may email this great opportunity to someone who would be a great fit for this role.

    All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.

    PeopleSearch Pte Ltd
    EA License No: 16S8057

  • 02 Jul 2019

    Senior Frontend Developer

    Singapore

    Permanent Position
    We are looking for talented Frontend Developers to join one of the leading MNC in the industry. As a Frontend Developer, you work will innovative and drive the digital transformation in the industry.

    Job Description

    • Design and develop quality responsive and interactive website (e-commerce / digital marketing) for the company
    • Stay abreast of the latest trends and suggest new features to enhance the application.
    • Collaborate with cross functional regional/global teams to look into continuous enhancement of good development practices.  
    • Commitment to code quality and optimize application performance.
    Expires on 19 Oct 2019

    Posted By

    Margaret Lee Hsin-Hua (Reg No: R1547495)

    Tel: +65 6738 6228

    margaretlee@peoplesearch.jobs

    Requirements

    • Bachelor’s degree or higher in Computer Science or related field.
    • At least 5 years of web frontend application development experience.
    • Must be specialized in least 1 of the JavaScript libraries and framework, such as Angular 5+, React, VueJs, jQuery, NodeJS and related technology.
    • Track record in delivering regional/global scale project(s).
    • Experience in e-commerce and digital marketing solutions will be a plus-point.
    • Experience with Agile development.
    • Working experience in a regional/global environment
    • Have good team spirit and accountable of work ownership; ability to work well with changing priorities; demonstrated flexibility and work with regional users.
    • 2 positions available

    Important Notes:

    • It is recommended to include relevant links/portfolios/project details to showcase your work in your resume.

     
    Location : Singapore
    Kindly indicate your current/last salary details and your notice period

    Interested candidates kindly forward your CV to margaretlee@peoplesearch.jobs (Margaret Lee Hsin-Hua, Reg No: R1547495).
    Feel free to forward this great opportunity to someone who would be a great fit for this role.

    All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.

    PeopleSearch Pte Ltd
    EA License No: 16S8057

  • 16 Feb 2019

    信頼性保証部門/品質保証部/インフォメーションマネジャー

    Japan

    Permanent Position
    アメリカ系製薬企業 - 深刻な病気を抱える患者さんを助けるための革新的な医薬品を開発し、提供することを使命とするグローバルなバイオファーマ製薬企業です。

    Job Description

    概要 (High-level Description; including manage team/individuals or not)
    ・ 安全性情報資材(市販後調査結果報告、添付文書改訂関連資料等)及び品質関連情報資材に関わる作成及び管理プロセスを最適化する。
    ・高品質な安全性情報資材(市販後調査結果報告、添付文書改訂関連資料等)及び品質関連情報資材を提供することにより、BMSKKのビジネスに貢献する。
    ・ 社内外ステークホルダーとの効果的なコミュニケーションを通じ円滑なオペレーションを行う。

    役割 (Roles & responsibilities)
    ・ 製品毎の戦略、国内外の規制要件であるGQP、GVP等及び社内手順書(GQP-SOP、GVP-SOP、Global SOP)に従い、高品質な品質関連情報資材ならびに安全性情報資材(市販後調査結果報告、添付文書改訂関連資料等)を提供するよう監督する。品質関連情報、添付文書/使用上の注意改訂のお知らせの資料作成、配布指示等を行う(以下に記載)。
     ・ 品質関連情報のお知らせの資料
     ・ 添付文書/使用上の注意改訂のお知らせの資料
     ・ 患者向医薬品ガイドの資料作成
     ・ 市販直後調査結果報告等の資料作成
     ・ 医療関係者向けweb siteに掲載する安全性情報の資料作成
     ・ 市販直後調査の計画を立案し、実施計画書の作成
     ・ 営業部門及びIT部門と連携し、市販直後調査を実施
     ・ 市販直後調査実施報告書の作成、提出
     ・ 薬事部門と連携し、一部変更申請や公知申請にあたり、市販後データの提供、資料作成
    ・ 厚生労働省、PMDA、東京都、提携他社のPMS部門、医療関係者等の社外のステークホルダーとの情報伝達関連業務に対応する。
    ・ 品質情報及び安全性情報伝達業務を円滑かつ効率的に遂行する。
    ・ 安全管理業務を独立して実施する。

    Expires on 18 Dec 2019

    Posted By

    Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 表記のメールアドレスまでご送付いただけますとスムーズです。)

    Tel: 08011184497

    nagai.m@peoplesearch.jobs

    Requirements

    必要な知識/スキル (Required knowledge/skills)
    1. Behavioral Skills (行動特性)
    以下の良好な行動特性を有する人材である
    ・ コミュニケーション
    ・ ネゴシエーション
    ・ リーダーシップ ビヘイビアの理解とそれに基づく行動能力
    2. Technical Skills (テクニカルスキル)
    ・ 国内規制(GCP/GVP/GPSP)及び欧米のPV規制に関する知識
    ・ 製品/治験薬に関する基礎知識
    ・ 当局から発出される通知の内容を理解できる。
    ・ 添付文書作成等の経験
    ・ 査察対応の経験
    ・ 業務遂行のための情報収集及び課題設定、改善提案能力
    ・ 照会事項対応を含めた当局対応の経験
    3. Experience (職務経験)
    ・ 3年以上のGVP/GPSPに関わる推進業務あるいはこれに類する業務の経験
    ・ 添付文書作成及びそれに付随する情報伝達業務の経験
    ・ 新薬製造販売の承認申請の経験
    4. Education/Certification (学歴/資格)
    ・ 理系大学の学士、または修士
    ・ 薬剤師免許があることが望ましい
    5. Language (語学力)
    ・ 業務上必要となる英語・日本語での文書作成能力及び口頭でのコミュニケーション力

  • 16 Feb 2019

    【研究開発本部バイオメトリクス】 Project Statistician (担当/担当課長/専門課長)

    Japan

    Permanent Position
    アメリカ系製薬企業 - 1876年に創業、140年を超える歴史がある。米国インディアナ州インディアナポリスに本社を置く、革新を追求する医薬品のリーディング・カンパニーです。世界各国の自社研究施設や外部の優れた科学的研究機関との提携による最新の研究成果を用いて、各治療領域で最高レベルの豊富なポートフォリオの医薬品を開発しています。世界120ヵ国以上で事業を展開しています。

    Job Description

    【職務概要/Overall Job Purpose】
    Provide strong statistical leadership in the process of drug development.
    The Project statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues. The Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.


    【主な職責/Primary responsibilities】
    Statistical Trial Design and Analysis
    ● Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.
    ● Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created.
    ● Collaborate with data management in the planning and implementation of data quality assurance plans.
    ● Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
    ● Participate in peer-review work products from other statistical colleagues.

    Communication of Results and Inferences
    ● Collaborate with team members to write reports and communicate results.
    ● Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
    ● Respond to regulatory queries and to interact with regulators.

    Therapeutic Area Knowledge
    ● Understand disease states in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

    Regulatory Compliance
    ● Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training. 

    Expires on 18 Dec 2019

    Posted By

    Miki Nagai ((少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 下記のメールアドレスまでご送付いただけますとスムーズです。) Tel: 080-1118-4497 nagai.m@peoplesearch.jobs)

    Tel: 080 1118 4497

    nagai.m@peoplesearch.jobs

    Requirements

    【必須経験(Required Experience (mandatory for hiring)】
    ◆ M.S. or Ph.D. in statistics or biostatistics.
    or
    ◆ Rich experiences in healthcare field as a statistician with science background such as mathematics or epidemiology.

    ◆ Ph.D. more preferable


    【望ましい経験/Desirable Experience】
    ◆ Experiences of collaboration with team outside of Japan (preferred: overseas living experience)


    【必須応募資格/Essential skills and license (mandatory for hiring)】
    ◆ Statistical and methodological knowledge in clinical development, epidemiology or related field.
    ◆ Regulatory knowledge of clinical trial methodology and statistics. 
    ◆ Ability to build relationships with individuals and teams.
    ◆ Strong English and Japanese communication and presentation skills


    【望ましい資格/Desirable skills and license】
    ◆ Proficient in the SAS programming language 

  • 14 Feb 2019

    Director, Legal & Compliance

    Japan

    Permanent Position
    MSDは、グローバルヘルスケアリーダーMerck & Co., Inc., Kenilworth, N.J., U.S.A.の一員として、日本の皆さまに医療用医薬品やワクチンをお届けし、革新的なヘルスケア・ソリューションを提供しています。強固なパイプラインと世界140カ国以上で事業を展開するグローバルなネットワークを活かし、未だ満たされていない日本の医療ニーズに積極的に応えていきます。

    Job Description

    Position Overview - Basic Functions & Responsibility
    The primary responsibility of Director, Legal & Compliance, is to provide legal & compliance consultation, guidance, advice and support to all divisions of the Company in Japan (“MSD Japan”), and to take a strong interest in understanding and implementing the Company’s compliance standards and managing compliance issues across all divisions. As a member of the Japan Legal & Compliance team and the broader Asia Pacific, China & Japan Legal & Compliance team, the individual shall handle legal matters and compliance issues arising from the Company in Japan, as directed by and under the supervision of the Executive Director, Legal & Compliance – Japan, collaborate closely with the Internal Control Officers (“ICOs”) of various functionsof MSD Japan, and work in conjunction with Regional and Global Legal & Compliance colleagues, external counsel and relevant headquarters and subsidiary staff and functional groups, as needed. 
    Primary Activities – Accountabilities, Supervision, 
    Primary activities include, but are not limited to:

    •Guide, monitor and assist with all activities of MSD Japan’s business that require legal/compliance input, and ensure all corporate, regional and local legal mandates and compliance objectives and goals of MSD Japan are met, with quality, collaborative and timely advice and oversight given to clients by both internal and external legal resources
    •Provide sound, appropriate and timely legal and compliance advice and oversight on proposals for new or revised initiatives/programs in MSD Japan, including but not limited to, patient programs, marketing initiatives, and other commercial proposals 
    •Collaborate with and provide guidance/support to each function in MSD Japan in the performance of their tasks and enable effective monitoring of compliance and related matters on behalf of MSD Japan
    •Work with Country Leadership Teams (“CLT”) of MSD Japan, as needed/directed, on risk assessments and implementation of continuous improvement on risk controls, provide insightful and strategic advice on business undertakings within the local and corporate compliance framework, and participate in meetings with the CLT as needed
    •Act as a resource and subject matter expert on Legal and Compliance issues, as well as the industry and the Company Compliance standards, policies and processes for the business organization in Japan and provide coaching and mentoring as needed, to newer and more junior members of the Japan Legal & Compliance team and ICOs
    •Lead or support new Legal and/or Compliance projects on behalf of MSD Japan, as directed by the Executive Director, Legal & Compliance – Japan and/or Regional/HQ Legal/Compliance management
    •Support the legal needs of key stakeholders through appropriate allocation and management of internal and external legal resources, provide business and other stakeholders, including ICOs, with adequate, high quality and pertinent legal advice and compliance input to ensure that MSD Japan complies with all legislative and regulatory requirements including privacy, anti-corruption/anti-bribery, fair competition and trade practice legislations, etc., as well as MSD’s policies, compliance standards and local industry guidelines
    •Assess, supervise and help manage the engagement of external legal resources in Japan and ensure that the service and advice received from external legal resources is timely, cost-effective and of consistently high quality
    •Understand and adapt changes in policies by the headquarters of the Company into local guidance and policy. Adopt external code and law changes into local SOP and practices by working with industry associations and external legal counsel
    •Proactively undertake and fulfill those tasks and activities designated for Legal & Compliance (“L&C”) for Japan, as shown in the Appendix, in consultation with and as directed by the Executive Director, Legal & Compliance – Japan 
    Company Leadership Standards applicable to the role include: 
    •Make Rapid, Disciplined Decisions - Make timely decisions at the right level with the right data, and support them once made.
    •Act with Courage & Candor - Speak openly, honestly and with conviction: have the courage to take appropriate risks and make difficult decisions.
    •Demonstrate Ethics & Integrity - Adhere to the highest standards of trustworthy and ethical behavior in all interactions and hold others to the same standards; comply with all laws, policies and regulations; identify and address ethical issues without hesitation.
    •Foster Collaboration - Actively listen and seek to understand differing perspectives; work together to achieve the common goals of the Company.
    •Focus on Customers & Patients - Focus the entire organization on delivering value for customers, including patients, by understanding and meeting their needs.
    •Drive Results – Set clear performance standards, overcome obstacles; hold ourselves and others accountable for achieving results.

    Expires on 16 Dec 2019

    Posted By

    Miki Nagai (Miki Nagai (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 下記のメールアドレス(nagai.m@peoplesearch.jobs )までご送付いただけますとスムーズです。) Tel: 080 1118 4497)

    Tel: 080 1118 4497

    nagai.m@pplesearch.com

    Requirements

    今回Complianceの方を主に担当いただくことになりますが、日本か他国の弁護士資格保有が必須となります。

    Skills, Knowledge, Experience & Qualifications required:
    •Admitted to practice law in Japan 
    •More than 10 years of post-admission legal/compliance experience
    •In-house legal and compliance experience in a large multinational pharmaceutical organization and/or commercial practice experience in a top tier law firm would be advantageous. .Language proficiency with English and Japanese required. 
    •Ability to pro-actively identify key issues and concerns and consistently apply a high standard of integrity, professionalism, legal knowledge and expertise and business ethics to achieve satisfactory resolution of such issues and concerns
    •Good knowledge and understanding of sales and marketing practices and applicable Code(s) of Conduct in the healthcare or pharmaceutical industry would be advantageous
    •Familiarity with the U.S. Foreign Corrupt Practices Act, the UK Bribery Act, and equivalent anti-corruption/anti-bribery laws in Japan would be advantageous
    •Strong working knowledge of privacy, competition and employment legislations highly desirable
    •Strong leadership and commitment to make sound and appropriate judgments 
    •Ability to think broadly with the best interest of the organization in mind
    •Ability to provide practical, commercially focused and value-added legal and compliance advice
    •Highly developed technical and research skills, ability to work independently and good attention for details 
    •Ability to lead a team of lawyers, paralegals and/or compliance professionals in adequately monitoring, supervising and guiding their duties and developing and maximizing their potential 
    •Ability to work collaboratively and lead, interact with and influence cross functional teams and senior management in the business, and to deal effectively with a broad range of people across all levels
    •Ability to design, implement, administer and advice on legal and/or compliance programs and procedures
    •Ability to effectively manage workflow, competing priorities and changing circumstances
    •Ability to work independently and prioritize work effectively under pressure
    •Ability to work autonomously as well as within a team environment
    •Strong analytical, drafting, negotiation and presentation skills, both in English and Japanese, including the ability to present to executive level management
    •Strong interpersonal and communication skills (both verbal and written), including the ability to conduct training, interviews and investigations, as needed
    •Technologically proficient, intermediate IT user skills
    •Strong solutions focused approach to problem solving
    •Proactive approach to streamlining compliance initiatives 
    •Ability to promote teamwork and open discussion of issues, coach and guide others
    •Ability to explain difficult issues and work to build alignment around complex or challenging situations
    •Proactive and responsive
    •Practical approach with a “can do” attitude

Job Application

First Name

Last Name

Contact No.

Email addresses

Upload your CV (File size up to 2MB only)

Choose File

Industry

Cancel