Medical Device & Diagnostics (MDD) Program Officer - Bali

Join Anugerah Pharmindo Lestari, a leading pharmaceutical and medical device distributor in Indonesia, as our Medical Device & Diagnostics (MDD) Program Officer based in Bali (Canggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, or Badung). In this role, you'll be at the forefront of driving our MDD program, ensuring our products meet the highest standards of quality and regulatory compliance. You'll work closely with healthcare professionals, manufacturers, and regulatory bodies to expand our market presence and enhance patient care.

Anugerah Pharmindo Lestari is a trusted name in the pharmaceutical industry, known for our commitment to excellence and innovation. As our MDD Program Officer, you'll have the opportunity to grow professionally and make a meaningful impact on the healthcare sector. Daily, you'll manage project timelines, coordinate with cross-functional teams, and ensure seamless operations from procurement to distribution.

📋 Tanggung Jawab Pekerjaan

• Manage and oversee the MDD program, ensuring adherence to regulatory standards and industry best practices.
• Coordinate with manufacturers, suppliers, and healthcare providers to source and distribute high-quality medical devices and diagnostics.
• Develop and implement strategies to expand market reach and enhance customer satisfaction.
• Monitor and report on program performance, identifying areas for improvement and innovation.
• Assist in training and development programs for staff to ensure they are equipped with the latest knowledge and skills.
• Collaborate with regulatory bodies to ensure compliance and maintain a strong reputation for quality and safety.
• Manage project timelines and budgets, ensuring efficient and effective use of resources.
• Build and maintain strong relationships with key stakeholders to drive business growth.

🎓 Kualifikasi & Syarat

• Bachelor's degree in Pharmacy, Medical Technology, or a related field.
• Minimum of 3 years of experience in the pharmaceutical or medical device industry, preferably in a program management or regulatory affairs role.
• Strong knowledge of Indonesian regulatory requirements for medical devices and diagnostics.
• Proficient in using project management tools such as MS Project, Trello, or Asana.
• Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
• Fluency in both English and Indonesian is a plus.
• Certification in regulatory affairs or quality management is a significant advantage.
• Ability to travel frequently to meet with stakeholders and attend industry events.

🛠️ Keahlian

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