PT Otsuka Indonesia

PT Otsuka Indonesia merupakan perusahaan farmasi yang telah berkiprah selama puluhan tahun dalam memproduksi dan memasarkan produk-produk kesehatan berkualitas tinggi. Fokus utama perusahaan ini adalah pada pengembangan cairan infus, obat etikal, nutrisi medis khusus, serta alat kesehatan. Dengan komitmen terhadap inovasi dan standar mutu internasional, PT Otsuka Indonesia telah berhasil membangun reputasi sebagai salah satu pemain utama di industri farmasi nasional.

Dalam proses produksinya, perusahaan ini menerapkan prinsip-prinsip Cara Pembuatan Obat yang Baik (CPOB), Cara Pembuatan Alat Kesehatan yang Baik (CPAKB), dan Cara Produksi Pangan Olahan yang Baik (CPPOB). Sertifikasi ISO seperti ISO 9001, ISO 22000, ISO 14001, dan ISO 50001 menjadi bukti nyata dari sistem manajemen mutu, keamanan pangan, lingkungan, dan energi yang dijalankan secara konsisten. Hal ini menunjukkan dedikasi perusahaan terhadap kualitas produk dan keberlanjutan operasional.

PT Otsuka Indonesia juga aktif melakukan ekspansi pasar ke berbagai negara di Asia dan Afrika. Produk-produknya telah diekspor ke negara-negara seperti Hong Kong, Singapura, Malaysia, Myanmar, Vietnam, Filipina, Mongolia, Sri Lanka, Thailand, India, dan Mesir. Langkah ini mencerminkan visi global perusahaan dalam menyediakan solusi kesehatan yang dapat diandalkan dan menjangkau lebih banyak masyarakat di berbagai belahan dunia.

Selain aspek bisnis, perusahaan ini juga menaruh perhatian besar pada tanggung jawab sosial dan pengembangan sumber daya manusia. Melalui berbagai program CSR yang berfokus pada isu kesehatan masyarakat, PT Otsuka Indonesia berupaya memberikan kontribusi nyata bagi peningkatan kualitas hidup. Filosofi perusahaan yang menekankan penciptaan produk baru demi kesehatan yang lebih baik menjadi landasan dalam setiap langkah strategisnya.

Lowongan Kerja PT Otsuka Indonesia

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.

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.

Penempatan Lawang, Jawa Timur

Batas Lamaran 16 Juni 2026

Cara Melamar :
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