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Required Quality Control (QC)- Associate -M.Sc. in Biotechnology, Molecular Biology, Microbiology, Biochemistry, Life Sciences, or a related discipline

CrisprBits Private Limited, Bangalore, India is Hiring  Quality Control (QC)- Associate  At CrisprBits, they are building CRISPR-based solutions across diagnostics and genome engineering, with quality and reliability at the core of everything we do. They are  hiring a Quality Control (QC) Associate who will play a key role in ensuring the consistency, performance, and compliance of their technologies, reagents, and diagnostic solutions through rigorous testing, validation, and quality control processes. Details are provided below  1. Designation:Quality Control (QC) Associate 2. Key Responsibilities:  -Perform in-process and final QC testing of CRISPR-based IVD kits and reagents Conduct quality testing of raw materials, consumables, and manufacturing batches -Maintain QC documentation, batch records, and test reports in compliance with ISO 13485 requirements -Support validation, verification, stability studies, and performance evaluation activities -Collaborate ...
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Required Quality Control (QC)- Associate -M.Sc. in Biotechnology, Molecular Biology, Microbiology, Biochemistry, Life Sciences, or a related discipline

CrisprBits Private Limited, Bangalore, India is Hiring  Quality Control (QC)- Associate 
At CrisprBits, they are building CRISPR-based solutions across diagnostics and genome engineering, with quality and reliability at the core of everything we do.
They are  hiring a Quality Control (QC) Associate who will play a key role in ensuring the consistency, performance, and compliance of their technologies, reagents, and diagnostic solutions through rigorous testing, validation, and quality control processes.
Details are provided below 
1. Designation:Quality Control (QC) Associate
2. Key Responsibilities: 
-Perform in-process and final QC testing of CRISPR-based IVD kits and reagents
Conduct quality testing of raw materials, consumables, and manufacturing batches
-Maintain QC documentation, batch records, and test reports in compliance with ISO 13485 requirements
-Support validation, verification, stability studies, and performance evaluation activities
-Collaborate with R&D, Production, and QA teams to investigate deviations and quality issues
-Ensure adherence to SOPs, GMP practices, biosafety guidelines, and internal quality standards
3.Eligibility Criteria: 
M.Sc. in Biotechnology, Molecular Biology, Microbiology, Biochemistry, Life Sciences, or a related discipline
4. Experience: 2-3 years of experience in Quality Control within molecular diagnostics, IVD, biotechnology, or life sciences laboratories
-Hands-on experience with DNA/RNA extraction, PCR, qPCR/RT-PCR, gel electrophoresis, and assay validation
-Familiarity with ISO 13485, GMP, and regulatory requirements for IVD products is preferred
-Experience with molecular diagnostic kits, nucleic acid amplification technologies, or CRISPR-based diagnostics will be an added advantage
-Detailed Job Description attached for reference.
5. How to Apply: 
Interested candidates may send their CV to: hr@crisprbits.com

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