Junior Manufacturing Biotechnologist

Join Amaris Consulting as a Junior Manufacturing Biotechnologist and play a pivotal role in advancing biopharmaceutical production in a state-of-the-art GMP environment. This is a unique opportunity to contribute to cutting-edge biotechnology processes while gaining invaluable experience in a dynamic and supportive team in Canggu. As a Junior Manufacturing Biotechnologist, you will work closely with senior colleagues to develop and optimize manufacturing processes, ensuring compliance with industry regulations and maintaining high standards of quality and safety.

Amaris Consulting is a leading consulting firm specializing in biopharmaceuticals, known for its innovative approach and commitment to excellence. Our state-of-the-art facilities in Canggu provide an ideal environment for you to grow and thrive. You will be part of a team dedicated to pushing the boundaries of biotechnology, working on projects that have a real impact on global health.

In your daily work, you will be responsible for executing standard operating procedures (SOPs), conducting process validations, and monitoring production parameters. You will use industry-standard tools such as LabVIEW, Excel, and SAP to ensure efficient and accurate data management. This role offers a fantastic opportunity to build a strong foundation in biopharmaceutical manufacturing and develop your skills in a supportive and collaborative environment.

📋 Tanggung Jawab Pekerjaan

• Execute standard operating procedures (SOPs) for biopharmaceutical production processes.
• Conduct process validations and troubleshooting to ensure compliance with industry regulations.
• Monitor and record production parameters using industry-standard tools such as LabVIEW, Excel, and SAP.
• Collaborate with cross-functional teams to optimize manufacturing processes and improve efficiency.
• Perform routine quality control tests and document results.
• Participate in continuous improvement initiatives to enhance production processes.
• Assist in the development and implementation of new manufacturing protocols.
• Maintain a clean and organized work environment in compliance with GMP standards.

🎓 Kualifikasi & Syarat

• Bachelor's degree in Biotechnology, Chemical Engineering, or a related field.
• 1-3 years of experience in a biopharmaceutical manufacturing environment.
• Familiarity with GMP regulations and quality assurance principles.
• Proficient in using LabVIEW, Excel, and SAP for data management and analysis.
• Strong analytical and problem-solving skills.
• Excellent communication and teamwork abilities.
• Ability to work in a fast-paced, detail-oriented environment.
• Certification in Good Manufacturing Practices (GMP) or a related field is a plus.

🛠️ Keahlian

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