Quality Control Technician I/II, RUO (ADX-59-20)
THE COMPANY: ArcherDX, Inc. - www.ArcherDX.com
ArcherDX is advancing molecular diagnostics with a robust technology platform for genetic mutation detection by next-generation sequencing. By combining patented Anchored Multiplex PCR (AMP™) chemistry in an easy-to-use, lyophilized format and powerful bioinformatics software, the Archer® platform enhance genetic mutation identification. ArcherDX provides oncology-focused research products and is pursuing regulatory approval for multiple companion diagnostic assays. ArcherDX is headquartered in Boulder, Colorado. Learn more at www.archerdx.com and follow @ArcherDXInc on Twitter, Facebook and LinkedIn.
- Execution of work instructions testing in-process raw, sub-assembly, and top-level materials
- Critical analysis of data ensuring compliance with standards
- Generation of data reports and release of materials
- Adherence to safety and quality laboratory standards
- Upkeep of personal training and associated records
- Maintenance of laboratory material stocks and initiation of re-orders
- Execution of validation protocols
- Identification of non-conforming material and subsequent report initiation and generation
- This position may cross-train in the GMP QC laboratories
- Review, understanding, and compliance with ArcherDX HIPAA Security policies and procedures.
- Safeguarding the privacy and security of protected health information and European Union personal data.
- Processing and handling of European Union personal data only as directed by ArcherDX for purposes of personalized molecular pathology.
- Drive and determination
- Ability to work in a fast-paced and dynamic environment
- Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance the success of the projects and maintain strong relationships within all parts of the company
- Strong communication and presentation skills
- Self-directed: needs little explicit direction
- Able to organize, prioritize, and delegate tasks to efficiently move projects forward.
- Level I: 0 - 2 or more years of experience in a laboratory setting
- Level II: 3 - 5 or more years of experience in a laboratory setting
- Experience utilizing micro-pipettes and PCR preferred for Level I and required for Level II
- Experience working in a GMP environment a plus
- Bachelor’s degree in a science-related field required