※ Submit your Application (Submit Your CV) to: https://linktr.ee/daewoong_pharmaceutical

Production Staff
Location: Cikarang

Responsibilities

• Qualification assessment of major manufacturing facilities for finished product pharmaceutical production team of biological products.
• Preparation of sterile process validation plans, execution, and reports.
• TF work performance such as qualification assessment, validation, and technology transfer of major manufacturing facilities for the setup of the Selatox new plant.
• Preparation and response to inspections as SME (Subject Matter Expert) during major global inspections.
• Sterile and non-sterile production of biological products/sterile finished products.
• Establishment and revision of SOPs and batch records.
• GMP work performance such as cause investigation, change management, and plan review using QMS systems.

Requirements

• Minimum Bachelor’s Degree or technical/vocational certification; Pharmacist qualification is an advantage.
• Previous experience in manufacturing, laboratory, biological, or sterile product settings is preferred.
• Knowledge of Good Manufacturing Practices (GMP) and safety regulations is a plus.
• Ability to work in a fast-paced environment and maintain attention to detail.
• Strong teamwork and communication skills, proficiency in English is a must, and Korean language proficiency will be considered a significant advantage.
• Willingness to work shifts and be placed in Cikarang.

※ Submit your Application (Submit Your CV) to: https://linktr.ee/daewoong_pharmaceutical