Are you passionate about driving quality excellence and technical innovation in a GMP-regulated environment? If so, this opportunity could be for you! Join us at B. Braun Indonesia, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare!  

As a Technical Officer (based in Karawang) with us in B.Braun, you will play a vital role in ensuring compliance and operational excellence within our Quality Management framework. You’ll drive continuous improvement, oversee calibration, and maintain packaging development standards in line with local and global regulations. Your responsibilities include managing qualification and validation activities, as well as supporting technical projects for new installations, equipment upgrades, and process improvements—ensuring timely execution and commercial readiness. This is a hands-on role where your technical expertise will directly impact product quality and patient safety.

Your Key Responsibilities: 

• Lead qualification and validation projects by defining risk analysis, creating protocols, organizing schedules, allocating resources, monitoring execution, and compiling reports in compliance with GMP and QMS standards.
• Coordinate external calibration and packaging development activities, including vendor sourcing, purchase requests, scheduling, and ensuring compliance with prerequisites for supplier visits.
• Maintain and update calibration and packaging material databases, ensuring accuracy and alignment with global and local regulatory requirements.
• Facilitate communication among stakeholders (suppliers, marketing, regulatory affairs, and quality teams) at local, regional, and global levels for calibration and packaging design matters.
• Manage internal technical administration, including KPI tracking, budget monitoring, purchase requisitions, asset management, and completion of RCA and CAPA from audits.
• Ensure compliance with all management systems (GMP, QMS, Halal Assurance System, SMK3, and HSE regulations), while supporting validation master plans and occupational health and safety requirements.

*The job function is not exhaustive and shall include any responsibilities as assigned by the Supervisor from time to time.

What you will bring to the team: 

• Associate or Bachelor Degree from Pharmacy, Pharmacist, Physics, Chemistry and Engineering background.
• Experience in validation, calibration and qualification. 
• Ideally 1 - 3 years of working experience in manufacturing processes and preferably from Pharmaceutical / Medical Devices; however, open to considering fresh graduates as well with the relevant background. 
• Knowledge in GMP policies and study.