job description
Join Erela as a Pharmaceutical Semisolid Production Supervisor and lead a dynamic team in ensuring the seamless production of high-quality semisolid pharmaceutical products. This role is pivotal in maintaining operational excellence, adhering to strict quality standards, and driving efficiency in our state-of-the-art manufacturing facility. If you are a results-driven professional with a passion for pharmaceutical manufacturing and leadership, this is your opportunity to make a significant impact in a growing industry.
Based in the vibrant regions of Bali, this position offers a unique blend of professional growth and work-life balance in one of the world's most sought-after destinations. You will oversee production processes, ensure compliance with CPOB (Cara Pembuatan Obat yang Baik) regulations, and collaborate with cross-functional teams to meet production targets while upholding the highest standards of quality and safety.
At Erela, we value innovation, integrity, and teamwork. As a supervisor, you will play a key role in fostering a culture of continuous improvement and operational excellence. If you are ready to take the next step in your career and contribute to the production of life-enhancing pharmaceutical products, we invite you to apply today.
Responsibility
- Lead and supervise the production team to ensure efficient and timely manufacturing of semisolid pharmaceutical products, including creams, ointments, and gels.
- Monitor and enforce compliance with CPOB (Good Manufacturing Practices for Pharmaceuticals) and other regulatory standards to ensure product quality and safety.
- Develop and implement production schedules to meet daily, weekly, and monthly targets while optimizing resource utilization.
- Conduct regular inspections of production lines, equipment, and facilities to identify and resolve potential issues that may impact productivity or quality.
- Collaborate with the Quality Assurance (QA) team to investigate and address any deviations, non-conformances, or customer complaints related to production.
- Train, mentor, and evaluate production staff to enhance their skills, performance, and adherence to company policies and procedures.
- Maintain accurate production records, including batch records, logs, and reports, to ensure traceability and compliance with documentation requirements.
- Drive continuous improvement initiatives by identifying opportunities to enhance efficiency, reduce waste, and improve overall production processes.
Qualifications
- Bachelor's degree in Pharmacy, Chemical Engineering, or a related field. A master's degree is a plus.
- Minimum of 3-5 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory role.
- In-depth knowledge of CPOB (Cara Pembuatan Obat yang Baik) and other relevant pharmaceutical regulations.
- Proven experience in managing production teams and ensuring adherence to quality standards in a GMP environment.
- Strong leadership, communication, and interpersonal skills to effectively manage and motivate a diverse team.
- Analytical and problem-solving skills to troubleshoot production issues and implement corrective actions.
- Proficiency in using production management software and Microsoft Office Suite.
- Ability to work in a fast-paced environment and adapt to changing priorities while maintaining attention to detail.