PJT cum Management Representative |requires a Pharmacy background
- Gaji
- Gaji tidak dicantumkan
- Jenis pekerjaan
- Penuh waktu
- Diposting
- Sumber
- Jobstreet Indonesia (SEEK API + GraphQL)
- kantor
Kami akan mengarahkan Anda ke situs tempat lowongan diposting untuk menyelesaikan lamaran.
Deskripsi pekerjaan
Location:Kawasan Industri Terpadu Batang, Kavling H10, Jalan Otomotif 1, Desa Ketanggan, Kecamatan Gringsing, Kabupaten Batang, Jawa Tengah 51281, Indonesia
About the role
This role is responsible for product registration, variation, and renewal, and for establishing and maintaining a quality management system in compliance with ISO 13485 and Indonesia CPAKB requirements. The position involves post-market surveillance of products, including adverse event reporting, product recalls, and field safety corrective actions, with compliant communication with regulatory authorities.
Key responsibilities
Responsible for product registration, variation, and renewal
Assist in establishing and maintaining a quality management system in compliance with ISO 13485 and Indonesia CPAKB requirements, ensuring that system documentation meets registration and regulatory inspection requirements
Responsible for post-market surveillance of products, including adverse event reporting, product recalls, and field safety corrective actions, and maintain compliant communication with regulatory authorities
Work closely with technical, production, and quality departments to ensure that product design changes, labeling, and instructions for use comply with registration requirements
Establish and maintain good relationships with the Indonesian Ministry of Health, medical device regulatory authorities, customs, and inspection and quarantine agencies; support local audits and ensure timely updates on regulatory policies
About you
Indonesian nationality, with fluent English in listening, speaking, reading, and writing
Bachelor's degree or above in Pharmacy; CPAKB certification is preferred
At least 3 years of experience in medical device regulatory registration, with strong knowledge of Indonesia's medical device registration processes and regulatory framework
Familiar with ISO 13485, MDR, FDA, and related standards
Good communication skills, with the ability to effectively engage with government officials and maintain strong relationships
Referensi: 206359 · Berlaku sampai 7 November 2026