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documentation molecular biology gmp glp quality control📋 Description
- Support reagents in the Clinical Laboratories.
- Prepare and qualify molecular diagnostic reagents.
- Perform QC tests on incoming raw materials.
- Review data for specification compliance.
- Maintain QC documentation and support QA activities.
- Ensure GLP/GMP compliance and cross-functional teamwork.
🎯 Requirements
- BS/BA in Biological Sciences or related field.
- 1+ years QC experience in a clinical lab preferred.
- Molecular biology and/or cell culture experience preferred.
- Strong attention to detail and problem-solving.
- Proficient in MS Word, Excel, PowerPoint.
- English proficiency and effective communication.
🎁 Benefits
- Comprehensive medical, dental, vision, life and disability benefits.
- Fertility care benefits and free testing for employees.
- Pregnancy and baby bonding leave.
- 401k plan and commuter benefits.
- Generous employee referral program.
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