OSD Production Supervisor

PT. Daewoong Pharmaceutical Indonesia; Cikarang; On-site; IDR 200,880,000 - 334,800,000; Full time

Job summary

PT. Daewoong Pharmaceutical Indonesia is seeking an experienced OSD Production Supervisor for our East Cikarang facility in West Java. This full-time role leads production activities, ensures quality, and maintains GMP compliance across oral solid dosage lines.

The candidate will manage production plans, supervise teams, and coordinate with SCM and other departments. Strong analytical and communication skills, plus experience in pharmaceutical manufacturing, are required.

Qualifications

• Minimum Bachelor Degree of Pharmacist.
• Minimum 5+ years of experience in pharmaceutical OSD production supervision or a similar supervisory role within manufacturing.
• Excellent problem-solving skills and the ability to make sound decisions under pressure.
• Strong organisational and planning abilities with the capacity to manage multiple priorities.
• Effective communication and interpersonal skills to work collaboratively with cross-functional teams.

Responsibilities

• Prepares/reviews GMP documents related to manufacturing.
• Creates/revises and reviews SOPs related to production.
• Manages data integrity per ALCOA principles throughout the life-cycle.
• Ensures batch records and SOPs align with manufacturing requirements.
• Monitors production plans with SCM and other departments; communicates issues and adjusts plans.

Skills

Leadership

Problem-solving

Communication

Planning

Team supervision

Education

Bachelor Degree in Pharmacy

Tools

Microsoft Office

Job description

About us

PT. Daewoong Pharmaceutical Indonesia is a leading pharmaceutical manufacturing company dedicated to producing high-quality medicines and healthcare products. As part of the Daewoong Group, we are committed to excellence, innovation, and maintaining the highest standards of quality and safety in everything we do. Our facility in East Cikarang, West Java, represents our investment in modern pharmaceutical manufacturing, and we pride ourselves on our professional team and rigorous operational standards.

About the role

We are seeking an experienced OSD Production Supervisor to join our manufacturing team at our East Cikarang facility in West Java. This is a full-time position that plays a critical role in ensuring the efficient, safe, and compliant operation of our oral solid dosage (OSD) production lines. As OSD Production Supervisor, you will be responsible for leading production activities, maintaining quality standards, and ensuring that all manufacturing processes meet pharmaceutical regulatory requirements. This role is essential to our mission of delivering safe and effective pharmaceutical products to our customers.

Key responsibilities

• Prepares/reviews various GMP documents related to manufacturing.
• Creates/revises and reviews SOPs related to production.
• Manages the generated manufacturing related data as per the ALCOA principle of conduct during the entire life-cycle to comply with data integrity.
• Checks that the intermediate product production was carried out as per the related SOP and manufacturing batch record, and reviews the manufacturing batch record.
• Checks the occurrence and completed status of the deviation on the product, which the manufacturing has been completed. If an abnormality occurs during the process, checks the matters and has the authority to proceed force start.
• Checks if the equipment issue during the process and trouble-shooting is being appropriately carried out.
• Creates/revises the production equipment Recipe as an intermediate manager.
• Reviews whether the manufacturing batch record has been appropriately prepared as per related document, when creating/revising.
• Establishes the production plan together with the related departments such as the SCM team, and manages the current production status. If an abnormality occurs from the production plan, shares with the related departments and organizes the production plan.
• Prepare and/or reviews pilot production protocol and report, and manufacturing batch records according to the production technology transfer.
• Monitors pilot production according to production technology transfer, and reviews the process standard settings.
• Prepare and/or reviews process validation protocol and report, and manufacturing batch records.
• Monitors process validation, checks the process standard settings and progress.
• Prepare and/or reviews the cleaning validation protocol and report.
• Checks if cleaning is carried out according to the cleaning validation protocol.
• Prepare and/or reviews the Qualification protocol and report, and checks if the verification has been carried out appropriately.
• Prepares/reviews URS related to the purchase/ maintenance of the new equipment, and proceeds the Impact Assessment.
• Conducts and completes production related education such as new employee training, OJT training, Plant GMP training, training for each department, problem prevention education and etc.
• Identifies the purchase list necessary for production and reflects in in the annual investment plan and proceeds the purchase following the purchasing process as per the annual investment plan (equipment, consumables, etc.). After completing the purchase through the purchasing system, registers the receipt and completes the settlement.
• Reviews/approves the manufacturing batch record of the batch which the manufacturing has completed.
• Carry out other jobs assigned by OSD Production Manager

What we’re looking for

• Minimum Bachelor Degree of Pharmacist.
• Minimum 5+ years of experience in pharmaceutical OSD production supervision or a similar supervisory role within manufacturing
• Proven experience in supervising production teams and managing personnel in a manufacturing environment
• Excellent problem-solving skills and the ability to make sound decisions under pressure
• Strong organisational and planning abilities with the capacity to manage multiple priorities
• Effective communication and interpersonal skills to work collaboratively with cross-functional teams

Preferred Qualification

• Good command in English especially in writing and speaking.
• Have fundamental knowledge in the manufacturing of pharmaceutical especially oral dosage form facility & production area.
• Have fundamental knowledge about GMP or other quality systems also good documentation practices and data integrity principles.
• Have knowledge of statistical data processing and able to read and evaluate data.
• Able to operate computer and Microsoft Office (word, excel, and power point).
• Understand and be proficient in the use of AI.

What we offer

We believe in supporting our employees' professional growth and wellbeing. PT. Daewoong Pharmaceutical Indonesia offers a competitive salary package, comprehensive health and safety benefits, and opportunities for career advancement within our growing organisation. We provide a structured work environment with clear expectations and support for professional development. Our team-oriented culture values dedication, continuous improvement, and excellence. We are committed to creating a workplace where skilled professionals can thrive and contribute meaningfully to our mission of producing quality pharmaceutical products. We encourage applications from qualified candidates and welcome discussions about how we can support your career goals.