OSD Tablet & Coating Specialist – Production

PT. Daewoong Pharmaceutical Indonesia; Cikarang; On-site; IDR 66,960,000 - 111,600,000; Full time

Job summary

PT. Daewoong Pharmaceutical Indonesia is seeking an OSD Production - Tableting & Coating Staff in East Cikarang, West Java. This full-time role operates and maintains equipment for tablet and capsule production, ensuring quality, efficiency, and compliance with GMP standards.

You'll manage documentation, batch records, IPC sampling, and data integrity while supporting CAPA, QMS deviations, and process validations. A strong background in pharmacy or related sciences is required.

Qualifications

• Bachelor or Master degree in Pharmacy, Engineering or Sciences.
• Pharmacist qualification preferred.

Responsibilities

• Prepares and double checks GMP documents related to manufacturing.
• Creates/revises SOPs related to production and accurately indicate the related documents.
• Manages manufacturing data per ALCOA throughout the lifecycle to ensure data integrity.
• Prepares/reviews manufacturing batch records and operates tableting & coating equipment.
• Collects samples for IPC per instructions and records results in batch records.
• Monitors processes to identify issues and implements recurrence prevention measures.
• Investigates deviations via QMS and defines preventive actions.
• Conducts CAPA, change control and training as per recurrence prevention.
• Executes pilot production for technology transfer.
• Performs Process Validation, Cleaning Validation, and Qualification recordings.
• Prepares/reviews URS for new equipment purchases.

Skills

GMP knowledge

Data integrity (ALCOA)

Statistical data processing

English language proficiency

Microsoft Office

AI awareness

Education

Bachelor/Master in Pharmacy

Engineering/Sciences background

Tools

Microsoft Office Suite

Job description

PT. Daewoong Pharmaceutical Indonesia is seeking an OSD Production - Tableting & Coating Staff in East Cikarang, West Java. This full-time role operates and maintains equipment for tablet and capsule production, ensuring quality, efficiency, and compliance with GMP standards.

You'll manage documentation, batch records, IPC sampling, and data integrity while supporting CAPA, QMS deviations, and process validations. A strong background in pharmacy or related sciences is required.