job description
Join Duopharma Biotech, Malaysia’s largest pharmaceutical GLC manufacturer, in our mission to advance oncology manufacturing and deliver life-saving treatments. As a Production Executive in our cutting-edge facility, you will play a pivotal role in ensuring the highest standards of quality, efficiency, and compliance in the production of oncology drugs.
This is a unique opportunity to contribute to a dynamic and innovative environment while enjoying competitive compensation, professional growth, and a comprehensive benefits package. If you are passionate about pharmaceutical manufacturing and eager to make a meaningful impact in the healthcare industry, we invite you to apply.
Relocate to Bali, Indonesia, and be part of a team that values excellence, collaboration, and continuous improvement.
Responsibility
- Oversee and coordinate daily production activities in oncology manufacturing to ensure adherence to GMP (Good Manufacturing Practices) and regulatory standards.
- Monitor production schedules, resource allocation, and workflow to optimize efficiency and meet deadlines.
- Collaborate with cross-functional teams, including Quality Assurance, R&D, and Supply Chain, to maintain seamless operations.
- Implement and enforce SOPs (Standard Operating Procedures) to guarantee product quality, safety, and compliance.
- Conduct regular audits and inspections to identify areas for improvement and ensure compliance with local and international regulations.
- Train, mentor, and supervise production staff to maintain high performance and adherence to protocols.
- Analyze production data and generate reports to track performance metrics, yield, and deviations.
- Participate in continuous improvement initiatives to enhance productivity, reduce waste, and streamline processes.
Qualifications
- Bachelor’s degree in Pharmacy, Chemical Engineering, Biotechnology, or a related field. Advanced degrees are a plus.
- Minimum 3-5 years of experience in pharmaceutical manufacturing, with a focus on oncology or sterile production preferred.
- Strong knowledge of GMP, FDA, PIC/S, and other regulatory requirements for pharmaceutical manufacturing.
- Proven leadership and project management skills, with the ability to manage teams and deadlines effectively.
- Excellent analytical, problem-solving, and communication skills.
- Proficiency in MS Office, ERP systems, and production management software.
- Familiarity with lean manufacturing, Six Sigma, or other process improvement methodologies is advantageous.
- Willingness to relocate to Bali, Indonesia and adapt to a fast-paced, high-compliance environment.