Clinical Regulatory Affairs Specialist

21 hours ago


Singapore GWIA PTE. LTD. Full time

Job Overview

We are seeking a highly skilled Clinical Regulatory Affairs Specialist to join our team at GWIA PTE. LTD.

About the Role

  • This is a $80,000 - $100,000 per year opportunity for a motivated and experienced professional to lead medical affairs initiatives and drive business growth.

Key Responsibilities

The successful candidate will be responsible for:

  • Collaborating with cross-functional teams to develop and implement strategic plans for medical activities, ensuring compliance with regulatory requirements.
  • Evaluating new concepts, ideas, licenses, and opportunities, providing medical expertise to ensure the proper development of new products and the optimal positioning and promotion of existing products.
  • Managing vendor relationships, including third-party HCP engagement platforms, Key Opinion Leaders (KOLs), and Health Care Organizations (HCOs) advocacy to build scientific credibility.
  • Supporting Medical Managers in the creation and tracking of promotional and non-promotional materials, as well as assisting with budget management.
  • Ensuring alignment with corporate standards, government regulations, and legal requirements.

Requirements

To be successful in this role, you will need:

  • A minimum of 1-3 years of experience in the Pharmaceutical/Healthcare Industry, preferably in medical affairs or management.
  • Working knowledge of regulatory requirements, standards, and internal quality documents.
  • A strong background in life sciences, with a preference for an MD, PharmD, or PhD degree.
  • Excellent communication and presentation skills, with fluency in English both written and verbal.
  • Basic computer literacy with competency in Microsoft Office suite.

What We Offer

We offer a competitive salary, comprehensive benefits package, and opportunities for growth and development in a dynamic and supportive environment.



  • Singapore HAYS SPECIALIST RECRUITMENT PTE. LTD. Full time

    Job Title: Regulatory Affairs SpecialistThe company is a fast-growing food and beverages business with a strong presence across Asia.Key Responsibilities:Develop and implement regulatory strategies to ensure compliance with all applicable laws and regulations.Stay up-to-date on changes in regulatory requirements and translate them into actionable steps for...


  • Singapore HAYS SPECIALIST RECRUITMENT PTE. LTD. Full time

    Regulatory Affairs Lead - SingaporeHAYS SPECIALIST RECRUITMENT PTE. LTD.About the CompanyHAYS SPECIALIST RECRUITMENT PTE. LTD. is a leading recruitment agency in Singapore, specializing in placing top talent in various industries. As a pioneer and growing team, we offer regional exposure, fast-track career progression into management, and exciting...


  • Singapore HAYS SPECIALIST RECRUITMENT PTE. LTD. Full time

    About the RoleWe are seeking a highly experienced Regulatory Affairs Lead to join our team in Singapore. The ideal candidate will have at least 5 years of experience in food regulatory affairs management, preferably with expertise in AMER or EMEA region.The successful candidate will be responsible for developing and implementing regulatory strategies to...


  • Singapore IQVIA Full time

    Key Responsibilities:Deliver regulatory projects on time and with a proactive approach, coordinating with in-country regulatory team leads.Core Competencies:Identify and interpret regulations, guidelines, and other pertinent information issued by regulatory agencies.Review scientific data, publications, and related papers to ensure compliance with...


  • Singapore HAYS SPECIALIST RECRUITMENT PTE. LTD. Full time

    Your new company Our client is a fast-growing food and beverages company, with a strong presence across Asia. They are looking for an experienced Regulatory Affairs Lead to help them grow their regulatory team here in Singapore. Your new role Below are some of the key responsibilities for the role: Develop and implement regulatory strategies to ensure...


  • Singapore INTERNATIONAL FLAVORS & FRAGRANCES (GREATER ASIA) PTE. LTD. Full time

    Roles & ResponsibilitiesJob SummaryThis position will be responsible for the management of product registrations, product compliance or product safety and risk assessment for Animal Nutrition & Health. IFF applies expert science to advance market-driven, healthy, and sustainable solutions for the food/feed, beverage, dietary supplements, and many other...


  • Singapore MTC CONSULTING PTE. LTD. Full time

    Job Description:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at MTC Consulting Pte Ltd.About the Role:This is an exciting opportunity for a talented professional to play a key role in ensuring compliance with regulatory requirements for medical devices.About the Company:MTC Consulting Pte Ltd is a leading consulting firm...


  • Singapore Airswift Full time

    Senior Regulatory Affairs Specialist (1-Year Contract) Location: Singapore (On-Site) We are seeking a Senior Regulatory Affairs Specialist to join a dynamic global healthcare organization specializing in innovative diagnostic solutions. This role focuses on regulatory submissions and license management across high-growth markets in the Asia-Pacific region....


  • Singapore MTC CONSULTING PTE. LTD. Full time

    We are seeking a highly skilled Regulatory Affairs Specialist to join our team at MTC Consulting Pte Ltd.Company OverviewMTC Consulting Pte Ltd is a leading consulting firm that provides expert advice on regulatory affairs in the medical devices industry. We are committed to helping our clients navigate the complex regulatory landscape and stay ahead of the...


  • Singapore PRESTIGE BIOPHARMA LTD Full time

    JOB FUNCTION Project Manager, Regulatory Affairs MAIN RESPONSIBILITIES Manage project submissions as assigned by Regulatory Affairs leadership Support the management of key projects, including execution, for submission, approval, and launch Review, prepare and author documents for regulatory submissions including clinical trial applications, marketing...


  • Singapore SL-Human Resource Consultancy Pte Ltd Full time

    SL-Human Resource Consultancy Pte Ltd is seeking a highly experienced Regulatory Affairs Director to oversee and manage all regulatory activities in Singapore.Estimated Salary: $120,000 - $180,000 per yearThis role will involve ensuring compliance with local and international regulations, developing regulatory strategies to support business objectives, and...


  • Singapore Baxter Full time

    Transforming Healthcare with BaxterBaxter is committed to making a positive impact on people's lives. As a Senior Regulatory Affairs Specialist, you will play a vital role in ensuring our medical devices meet the highest regulatory standards.Key Responsibilities:Develop and execute regulatory project plans to ensure timely submission of documents to...


  • Singapore SG Diagnostics Full time

    Communicate with regulatory bodies on regulatory affairs (e.g. product registration, change notifications) Communicate with team members on required regulatory requirements during product development Dossier preparation and submission for product registration Support post-market activities (e.g. customer complaint, post-market surveillance, adverse events,...


  • Singapore PRESTIGE BIOPHARMA LIMITED Full time

    Prestige Biopharma Limited is seeking an experienced Regulatory Affairs Project Lead to join our team.About the RoleWe are looking for a highly skilled and motivated individual to lead regulatory affairs projects from submission to approval, ensuring timely delivery and quality results.The successful candidate will have at least 3-5 years of experience in...


  • Singapore MTC CONSULTING PTE. LTD. Full time

    Company OverviewMTC Consulting Pte Ltd is a leading provider of consulting services for medical devices and life sciences technology.SalaryThe estimated salary for this role is $4,500 + completion bonus, with the potential for conversion to a permanent role. This offer is based on industry standards in Singapore and the specific requirements of the...


  • Singapore PRESTIGE BIOPHARMA LIMITED Full time

    Roles & ResponsibilitiesJOB FUNCTIONProject Manager, Regulatory AffairsMAIN RESPONSIBILITIES· Manage project submissions as assigned by Regulatory Affairs leadership· Support the management of key projects, including execution, for submission, approval, and launch· Review, prepare and author documents for regulatory submissions including clinical trial...


  • Singapore NYPRAX PHARMA PTE. LTD. Full time

    Job OverviewWe are seeking an experienced Regulatory Affairs Manager to join our team at NYPRAX PHARMA PTE. LTD.This is a challenging role that requires strong regulatory knowledge and excellent communication skills.The successful candidate will be responsible for coordinating and submitting documentation to the Health Sciences Authority, compiling client...


  • Singapore Avanos Full time

    Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at Avanos. As a key member of our regulatory department, you will be responsible for ensuring compliance with regulatory requirements in the assigned markets throughout the product lifecycle.Main...


  • Singapore SL-Human Resource Consultancy Pte Ltd Full time

    Job OverviewWe are seeking an experienced Regulatory Affairs Director to join our team in Singapore.Job Description:Key Responsibilities:Compliance and Submissions:Oversee the preparation, submission, and maintenance of regulatory filings and submissions to health authorities.Ensure compliance with local, regional, and international regulatory...


  • Singapore INTEGRITY PARTNERS PTE. LTD. Full time

    About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at INTEGRITY PARTNERS PTE. LTD.This 6-month contract position involves assisting in the execution of regulatory strategies for medical devices across various markets, with a focus on efficient pre-market and post-market approvals.