Di awal berdirinya pada tahun 1997, Otsuka merupakan perusahaan afiliasi dari Otsuka Pharmaceutical Co, Ltd Jepang yang memulai perjalanannya di Indonesia dengan nama PT Kapal Indah Otsuka. Perusahaan ini terbentuk dari hasil investasi bersama antara Otsuka Pharmaceutical Jepang dan PT Kapal Api dengan Pocari Sweat sebagai produk pertamanya. Kemudian di tahun 1999, PT Kapal Indah Otsuka merubah namanya menjadi PT Amerta Indah Otsuka.
Semakin berkembangnya perusahaan, pada tahun 2004 PT Amerta Indah Otsuka membuka pabrik pertama yang terletak di Sukabumi, Jawa Barat menyusul 6 tahun berikutnya pabrik Pocari Sweat di Kejayan, Pasuruan, Jawa Timur didirikan. Dengan keberhasilannya dalam memasarkan produk, hingga kini produk yang dihasilkan telah didistribusikan di seluruh Indonesia. PT Amerta Indah Otsuka gencar melakukan pendistribusian baik secara langsung melalui kantor cabang resmi maupun distributor-distributor yang tersebar di seluruh Indonesia dan Asia Tenggara.
Seiring dari kemajuan perusahaan, Otsuka berkomitmen untuk terus meningkatkan kualitas dengan mengimplementasikan Sistem Manajemen Mutu ISO 9001:2015, Sistem Keamanan Pangan ISO 22000: 2015, dan Sistem Manajemen Lingkungan ISO 14001: 2015.
Lowongan Kerja PT Amerta Indah Otsuka
Tertarik dengan Lowongan Kerja PT Amerta Indah Otsuka? Siapkan berkas lamaran dan CV anda beserta berkas pendukung lamaran lainnya. Simak kualifikasi dibawah ini:
1. Audit, QRM & Compliance Staff
Job Description:
PT Otsuka Indonesia is seeking a dedicated QA Audit, QRM & Compliance Staff to support quality systems, risk management, and compliance programs. This role is responsible for coordinating quality risk management activities, vendor qualification, compliance reviews, and maintaining quality documentation to ensure adherence to GMP standards.
We are looking for candidates who are analytical, detail oriented, and passionate about quality culture and regulatory compliance in pharmaceutical manufacturing.
Key Responsibilities:
- Support Quality Risk Management (QRM) activities and risk assessment reviews.
- Conduct vendor qualification and support vendor audit programs.
- Review and maintain quality system documents and Quality Manual.
- Support compliance initiatives, CAPA follow up, and contamination control programs.
Requirements:
- Education: Bachelor’s degree (S1) in Pharmacy or registered Pharmacist (Apoteker).
- Experience: Minimum 1 years of relevant experience are preferred, fresh graduates with relevant competencies are welcome to apply.
Preferred Skills:
- Good understanding of GMP, especially CPOB, QRM and US FDA requirements.
- Knowledge of vendor management, CAPA, and audit process.
- Strong documentation, analytical, and problem solving skills.
- Proficient in English and Microsoft Office applications.
2. Validation & Qualification Staff
Job Description:
PT Otsuka Indonesia is seeking a dedicated QA Validation, Qualification & Project Staff to support validation and qualification activities across manufacturing facilities and quality systems. This role is responsible for executing validation master plans, preparing validation and qualification protocols, and ensuring compliance with GMP requirements throughout project implementation.
We are looking for candidates with a strong pharmaceutical background, attention to detail, and a passion for Quality Assurance and continuous improvement in pharmaceutical manufacturing.
Key Responsibilities:
- Support Validation Master Plans and qualification activities.
- Prepare and review validation and qualification protocols and reports.
- Monitor calibration activities and ensure compliance with GMP requirements.
- Participate in project implementation and continuous improvement initiatives.
Requirements:
- Education: Bachelor’s degree (S1) in Pharmacy or registered Pharmacist (Apoteker).
- Experience: Minimum 1 years of relevant experience are preferred, fresh graduates with relevant competencies are welcome to apply.
Preferred Skills:
- Good understanding of GMP, especially CPOB and US FDA requirements.
- Knowledge of validation, qualification, calibration, and pharmaceutical process.
- Strong documentation, analytical, and problem solving skills.
- Proficient in English and Microsoft Office applications.
Simak Juga : Lowongan D3 Semua Jurusan Posisi Lainnya
Cara Melamar:
Jika Anda salah satu kriteria yang ada di kualifikasi lowongan kerja ini, Silahkan daftar secara online:
| 1. Audit, QRM & Compliance Staff | DAFTAR |
| 2.Validation & Qualification Staff | DAFTAR |
Pendaftaran dibuka hingga: 16 June 2026
Head Office:
Pondok Indah Office Tower 1 Lantai 8
Jl. Sultan Iskandar Muda Kav. V – TA, Jakarta Selatan
Factory:
Jl. Sumber Waras No. 25, Lawang, Malang
*hanya yang memenuhi kualifikasi yang akan di proses
Proses rekrutmen & seleksi pelamar tidak dipungut biaya apapun
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