Job Description
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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) 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.
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.
Qualifications
Associate or Bachelor Degree in Pharmacy, Pharmacist, Physics, Chemistry, or Engineering background.
Experience in validation, calibration, and qualification.
1–3 years of working experience in manufacturing processes, preferably from Pharmaceutical / Medical Devices; open to fresh graduates with the relevant background.
Knowledge of GMP policies and studies.
Benefits
Annual bonus
Company devices provided
Education support & personal development
Onsite canteen
Medical Insurance
Annual Leave
Regular team building and employee social gatherings
What’s next?
Upon receiving your application, our dedicated Talent Acquisition team will meticulously review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead into our seamless onboarding experience. Join us and be part of something extraordinary!
We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are.
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