Performing QC testing and validation following written procedures using GMP compliance.
Performing material incoming QC, in-process testing, and final product release.
Preparing reagents, buffers, standards, samples, and controls according to approved procedures.
Multitasking effectively and efficiently to ensure maximum and high-quality output.
Maintaining cleanliness and orderliness of work area.
Performing assay development task based on the project.

🎯 Requirements

BS in biology, chemistry, biochemistry, or other related science.
0 - 2 years’ experience in the related IVD or biotech field.
High level of integrity, flexible, action oriented.
High attention to detail, excellent organizational skills, and ability to work on multiple projects.
Ability for problem-solving and decision-making.
Excellent interpersonal and verbal communications skills.

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