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Star Med

Verified This Company has been
Verified or Registered as Real.
This Company has been
Verified or Registered as Real.
အကြောင်းအရာ
အလုပ်များ 2
အကြောင်းအရာ Star Med

အလုပ်ရှင်၏ အသေးစိတ်အချက်အလက်များ

  • အမျိုးအစား: Direct Employer
  • လုပ်ငန်းအမျိုးအစားများ: Biotechnology/Pharmaceuticals, Medical/Hospital, Pharmaceutical/Life Sciences
  • ဝန်ထမ်းအရေအတွက်: 51 to 100

လိပ်စာ

No.313/B, Mya Nandar Street, Bauk Htaw, Yankin Township, Yangon.,ရန်ကုန်တိုင်း, Myanmar

ကျွန်တော်တို့ ဘာတွေလုပ်သလဲ

Distribution and Trading of Healthcare Products.
All Star Med Jobs
Job Summary We are seeking a Product Executive to support medical product promotion, market growth, and customer engagement for Star Med in Yankin, Yangon. This role suits an experienced professional who can work closely with healthcare stakeholders and internal teams. Key Responsibilities ● Conduct product and role-play training for the Marketing & Sales Team, including promotion staff. ● Visit KOL doctors and modern trade outlets to share product knowledge. ● Organize Medical CMEs, KOL doctor dinners/lunches, and health talk projects with public health speakers. ● Deliver product presentations at YCH, YGH, and modern trade outlets. Support the creation and execution of go-to-market strategies, including product positioning, pricing, and messaging. ● Coordinate with Digital marketing team and manage company Facebook pages, create monthly content, and execute digital promotions. Develop brochures, pamphlets, catalogs, and insert papers for new products. ● Analyze competitors, build competitor profiles, and enhance brand awareness with influencers and bloggers.
Job Summary Star Med is seeking a detail-oriented professional to coordinate regulatory and logistics-related activities in support of pharmaceutical operations. This role ensures timely documentation, compliance, and cross-functional coordination to keep products moving efficiently. Job Description 1. Manage both pharmaceuticals and medical device products across Asia. 2. Communicate with regulatory bodies on regulatory affairs (e.g., product registration, change notifications) 3. Review, format all documents and responses prior to submitting to the FDA and also prepare and submit new online drug, medical device registration to FDA. 4. Analyze label, ACTD dossier guidance, and regulatory compliance, regulation decisions before submission to FDA to identify trends and gaps or alignment in our current regulatory strategy in FDA and maintain regulatory files. 5. Provide regulatory advice to project teams and key internal / external stakeholders for start-up and maintenance activities in the projects. Ensures high quality of all regulatory documents. 6. Manage team to ensure that all submissions and responses to competent authorities and Ethic Committees and are tracked in a timely manner 7. Act as primary point of contact for regulatory activities for the supply chain.
Star Med ဆုများ