Production Supervisor (Pharmaceutical Manufacturing)

PT Medifarma Laboratories; Depok; On-site; IDR 89,280,000 - 133,920,000; Full time

Benefits offered by this job

Opportunities for professional growth

Collaborative work environment

Employee wellness programs

Job summary

PT Medifarma Laboratories in Depok, West Java, seeks a Production Supervisor to oversee the daily pharmaceutical production line, ensure GMP/compliance, and drive quality and efficiency across operations.

The ideal candidate has an apothecary background with 2–3 years’ experience, strong leadership and English skills, thorough knowledge of production equipment and QC standards, and a proven team leadership track record.

Qualifications

• A apothecary background with 2–3 years of experience.
• Knowledge of GMP and Halal/QA standards.
• Strong leadership and communication skills in English.
• Experience with pharmaceutical production processes and QC.
• Ability to lead and motivate a team in a production setting.

Responsibilities

• Supervise daily operations of the pharmaceutical production line.
• Prepare and control product schedules and WIP inventory.
• Oversee GMP implementation, SOPs, and Halal guarantees.
• Perform product checkups and maintain process records.
• Create/ revise SOPs for processing area.
• Coordinate with Engineering, QA/QC, PPIC for smooth production.
• Troubleshoot packaging issues with Production Manager.

Skills

Leadership

GMP knowledge

English

Quality consciousness

Problem solving

Team management

Regulatory familiarity

Counting

Education

Apothecary certificate

Job description

Production Supervisor (Pharmaceutical Manufacturing)

Join PT Medifarma Laboratories' dynamic team as a Production Supervisor based in Depok, West Java. In this full-time position, you will play a crucial role in overseeing and optimising the pharmaceutical production process to ensure the highest standards of quality and efficiency.

Requirements

• Apothecary with minimum 2 - 3 years working experiences
• Have received training and understand the Good Manufacturing Practices (CPOB)
• Strong interpersonal skill and leadership capability
• Required language(s): English
• Skilled and thorough in counting
• have experience on solid granulation products
• Strong technical knowledge of pharmaceutical production processes, equipment, and quality control standards
• Excellent problem-solving and decision-making skills to address production challenges effectively
• Proven ability to lead and motivate a team, fostering a collaborative and high-performing work environment
• Familiarity with relevant regulatory requirements and quality management systems

Job Description

• Supervise and coordinate the daily operations of the pharmaceutical production line, ensuring adherence to standard operating procedures and quality control measures
• To prepare/control product schedule and work in process product in the area
• To control/supervise implementation of GMP (Good Manufacturing Pactice, SOP and Halal guarantee system
• Carry out a consummation check of the product that is being made.
• Create a Work In Process list
• Resolving problems that arose during the packaging process (troubleshooting) with the Production Manager
• Create / revise the SOP used in the processing area
• Coordinating with the Engineering, QA / QC, PPIC for smooth processing

What we offer

At PT Medifarma Laboratories, we are committed to providing our employees with a rewarding and fulfilling work experience. In addition to a competitive salary, we offer a range of benefits, including:

• Opportunities for professional development and career advancement
• Collaborative and supportive work environment
• Employee wellness and team-building activities

About us

PT Medifarma Laboratories is a leading pharmaceutical company, dedicated to developing and manufacturing high-quality healthcare products. With a strong focus on innovation and excellence, we are committed to improving the well-being of our customers and communities. Join our team and be a part of our exciting journey as we continue to shape the future of the pharmaceutical industry.

Medifarma Laboratories is a pharmaceutical company based in Indonesia and an affiliate of United Laboratories, Inc., the biggest pharmaceutical company in the Philippines and a sister company of Darya-Varia Laboratoria, Indonesia. With its head office in Depok, on the southern outskirts of Jakarta, Indonesia's capital, the Medifarma production facility is located in a complex that houses such big-name multinational pharmaceutical companies as Bayer Health Care, Glaxo Smith Kline, Pfizer, etc.

Founded in 1975, our original production facility extended to 36,595 m2. It was expanded by 14,164 m2 in 1992 in line with the company’s growth so as total floor space is currently 50,759 m2.

Our production facility and operations have been certified by the Indonesia NADFC (National Agency of Drug and Food Control), with standards of manufacturing practice found to be in accordance with the current standard of Good Manufacturing Practices as well as to meet the standard required by Pharmaceutical Inspection Co-operation Scheme (PIC/s) and World Health Organization (WHO).

Medifarma exports its products to affiliates in the Philippines, Singapore, Malaysia, Hong Kong, Myanmar and Cambodia. We are committed to maintaining the highest quality standards for everything we produce

Medifarma Laboratories is a pharmaceutical company based in Indonesia and an affiliate of United Laboratories, Inc., the biggest pharmaceutical company in the Philippines and a sister company of Darya-Varia Laboratoria, Indonesia. With its head office in Depok, on the southern outskirts of Jakarta, Indonesia's capital, the Medifarma production facility is located in a complex that houses such big-name multinational pharmaceutical companies as Bayer Health Care, Glaxo Smith Kline, Pfizer, etc.

Founded in 1975, our original production facility extended to 36,595 m2. It was expanded by 14,164 m2 in 1992 in line with the company’s growth so as total floor space is currently 50,759 m2.

Our production facility and operations have been certified by the Indonesia NADFC (National Agency of Drug and Food Control), with standards of manufacturing practice found to be in accordance with the current standard of Good Manufacturing Practices as well as to meet the standard required by Pharmaceutical Inspection Co-operation Scheme (PIC/s) and World Health Organization (WHO).

Medifarma exports its products to affiliates in the Philippines, Singapore, Malaysia, Hong Kong, Myanmar and Cambodia. We are committed to maintaining the highest quality standards for everything we produce