Custom Quality Analyst II
About The Position
The Custom Quality Analyst II is responsible for evaluating products in support of all manufacturing areas within Integrated DNA Technologies in accordance with ISO 9001, ISO 14001 and ISO13485 requirements. This evaluation involves performing in-process and final QC testing to determine the pass/fail status of products by using a wide variety of molecular biology methods and specialized equipment. This position reports to the Manager of Custom Quality Control, is part of the Custom Quality Control department located in Coralville, IA and will be an on-site role. Schedule: Monday -Thursday, 7am to 5:30PM
Requirements
- Bachelor’s degree in a science related field required. (Biology, Genetics, Chemistry or related life science field preferred); Alternatively, an associate’s degree with 2 years of directly related experience.
- At least 2 years applicable lab experience.
- Ability to lift, move or carry equipment up to 35lb
Nice To Haves
- Previous experience in PCR and qPCR
- Next Generation Sequencing
- Enzymatics
Responsibilities
- Perform and analyze a variety of QC tests according to Standard Operating Procedures and accurately document results via established product specifications.
- Perform data entry and peer review for accuracy in accordance with lab procedures.
- Perform maintenance and calibration on a variety of specialized equipment and assist in troubleshooting as needed.
Benefits
- paid time off
- medical/dental/vision insurance
- 401(k)
- bonus/incentive pay
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
