Yuannita Citra
Branch Administrator @ PT Itama Ranoraya Tbk
About
I am a Pharmacist with over five years of experience in the pharmaceutical and medical device industry, currently serving as a Technical Responsible Person ensuring full compliance with Ministry of Health regulations, CPAKB, CDAKB, and ISO 13485 standards. Experienced in regulatory compliance, internal and external audits, SOP development, technical documentation control, quality assurance, and managing NIE and TKDN submissions. Skilled in cross-functional coordination to build efficient and compliant production systems. Recognized as a structured, communicative, and detail-oriented professional, I am open to opportunities in Regulatory Affairs, Quality Assurance, and Operational Compliance within the medical device sector.
Indonesia
Bandung
Medical Device
Accounts Receivable (AR), Operations Management, Pharmacy Practice, Inventory Management, Patient Counseling, Leadership, Office Administration, Corporate Communications, Regulatory Compliance, Cross-functional Coordination, Time Management, Critical Thinking, Medical Device Regulation (MDR), Document Management, Quality Assurance, Communication, Kemampuan Berorganisasi, Komunikasi, Regulatory Affairs, Microsoft Excel
Experience

Branch Administrator
Бандунг
As a Branch Admin in a medical devices distribution company, responsible for managing end-to-end administrative processes and controlling document flow across the branch, both with the head office and customers. Overseeing order processing from purchase order receipt through to delivery coordination, while ensuring completeness and compliance of documentation for customer transactions. Providing administrative support to the Branch Manager in daily operations, as well as monitoring and reconciling branch sales and payment data accurately and in a timely manner

Penanggung Jawab Teknis Produksi
Bandung, Jawa Barat, Indonesia
Bertanggung jawab memastikan seluruh proses produksi dan distribusi alat kesehatan sesuai regulasi Kementerian Kesehatan, termasuk penerapan CPAKB, CDAKB, dan ISO 13485. Mengawasi kepatuhan proses penanganan bahan baku, produksi, pengemasan, distribusi hingga penanganan keluhan sesuai standar mutu dan dokumentasi teknis. Menyusun, mereview, dan menerapkan SOP lintas divisi (Produksi, QA, HR, Marketing) agar selaras dengan ketentuan regulator. Terlibat dalam audit internal/eksternal, sertifikasi, serta pengurusan dokumen seperti NIE dan TKDN. Mengkoordinasikan tim dan memastikan sistem dokumentasi berjalan efisien, akurat, dan sesuai persyaratan Kemenkes.

Penanggung Jawab Teknis Produksi
Bandung, Jawa Barat, Indonesia
Bertanggung jawab memastikan seluruh proses produksi dan distribusi alat kesehatan sesuai regulasi Kementerian Kesehatan, termasuk penerapan CPAKB, CDAKB, dan ISO 13485. Mengawasi kepatuhan proses penanganan bahan baku, produksi, pengemasan, distribusi hingga penanganan keluhan sesuai standar mutu dan dokumentasi teknis. Menyusun, mereview, dan menerapkan SOP lintas divisi (Produksi, QA, HR, Marketing) agar selaras dengan ketentuan regulator. Terlibat dalam audit internal/eksternal, sertifikasi, serta pengurusan dokumen seperti NIE dan TKDN. Mengkoordinasikan tim dan memastikan sistem dokumentasi berjalan efisien, akurat, dan sesuai persyaratan Kemenkes.

Executive Assistant
ELVINDO GROUP
Jakarta, Indonesia
Mendukung kinerja Direktur dalam pengelolaan operasional dan administrasi perusahaan. Menyusun notulensi rapat, menyiapkan dokumen penting, dan mengatur jadwal serta komunikasi lintas divisi. Mengelola arsip perusahaan, kontrak kerja sama, serta laporan administrasi dan keuangan sederhana. Berperan sebagai penghubung antara manajemen, karyawan, dan pihak eksternal untuk memastikan kelancaran operasional harian.

Apoteker Penanggung Jawab
Century Healthcare (CHC)
Jakarta, Indonesia
Bertanggung jawab atas seluruh kegiatan pelayanan farmasi dan pengelolaan obat di apotek sesuai peraturan BPOM dan standar kefarmasian. Melakukan pelayanan resep dan konseling pasien untuk memastikan penggunaan obat yang aman dan rasional. Mengelola stok obat, penyimpanan, serta administrasi gudang sesuai ketentuan Cara Distribusi Obat yang Baik (CDOB). Menyusun laporan rutin dan memastikan kepatuhan terhadap peraturan perizinan dan pelaporan ke instansi terkait. Melatih dan mengawasi asisten apoteker dalam pelayanan harian.
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