Temporary QC Associate II
Maravai LifeSciences
Summary
Maravai LifeSciences is seeking a Temporary QC Associate II to join the QC team. This role is primarily responsible for routine testing of raw materials, in-process materials, final products, coordinating outsourced testing with contract labs, and routine data review of test results in a quality control laboratory.
Job description
How you will make an impact
- Routinely operate analytical UHPLC, mass spectrometer, pH/conductivity meter, qPCR, dot blot, UV-vis spectrometer, FTIR, Fragment Analyzer, and restriction digests.
- Daily planning of QC testing from various departments using FileMaker and other internally created scheduling tools.
- Routine workup and delivery of test results.
- Aid in peer review of testing data and write-ups of other technicians for accuracy and completeness.
- Coordinate outsourced tests with various contract labs for core manufacturing and GMP labs from sample submission to delivery of test results.
- Review instrument, performance qualification, and calibration logs for accuracy, completeness, and in accordance with GDP and internal requirements.
- Assist in the daily management of QC laboratory supplies and raw materials.
- Maintain instrument logs.
- Perform daily and weekly maintenance of instruments per SOP.
- Contribute to preparation and updating of QC standard operating procedures.
- Maintain meticulous documentation of all Quality Control records.
- Maintain lab housekeeping, organization, and inventory supply.
- Perform other functions and duties as required.
The skills and experience that you will bring
- B.S. or advanced degree in chemistry or biology or a related science required with 3-6 years of relevant experience.
- Hands-on experience with any of the following instrumentation: HPLC, Mass Spec, qPCR, UV-Vis spectrophotometer, Fragment Analyzer.
- Familiar with Chromatography Data Systems (i.e. Chromeleon) a plus.
- Computer skills (Database software, Microsoft Office Suite).
- Excellent communication skills (Email, Phone).
- Requires knowledge of and experience using GLP or cGMP principles.
- Working knowledge of standard chemical safety/hygiene requirements and overall safe workplace practices, especially in a laboratory setting.
Requirements
- B.S. or advanced degree in chemistry or biology or a related science
- 3-6 years of relevant experience
- Hands-on experience with HPLC, Mass Spec, qPCR, UV-Vis spectrophotometer, or Fragment Analyzer
- Knowledge of and experience using GLP or cGMP principles
- Working knowledge of standard chemical safety/hygiene requirements
- Computer skills (Database software, Microsoft Office Suite)
- Excellent communication skills (Email, Phone)
Benefits
- Medical Plans
- HSA/FSA Options
- Fertility & Family Planning Assistance
- Pet Insurance
- Retirement Contributions
- Holidays & Paid Time Off
- RSU Grants
- Employee Stock Purchase Plans
Company overview
Maravai LifeSciences is a leading life sciences company founded in 2014 and headquartered in San Diego, California. The company provides critical products and services that enable the development of groundbreaking vaccines, drug therapies, cell and gene therapies, and diagnostics. Maravai's solutions empower research into human diseases and support the entire biopharmaceutical development process from early discovery through commercialization. The company operates through several key brands including TriLink BioTechnologies (specializing in RNA synthesis and mRNA production), Glen Research (DNA and RNA oligonucleotide synthesis reagents), Cygnus Technologies (bioprocess impurity detection), and Alphazyme (molecular biology enzymes). With approximately 550-1,000 employees, Maravai holds numerous patents and offers over 1,500 innovative products and services, including their proprietary CleanCap® mRNA capping technology. The company serves top global biopharmaceutical companies, emerging biotech firms, academic research institutions, and in vitro diagnostics companies, playing a crucial role in advancing life sciences innovation worldwide.