Temporary QC Associate II
TriLink Biotechnologies
Summary
Maravai LifeSciences is seeking a Temporary QC Associate II to join our 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. This successful candidate will thrive in a flexible fast-paced environment and demonstrate excellent attention to detail.
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 a FileMaker and other internally created scheduling tools.
- Routine workup and delivery of test results.
- Aid in peer reviewer of testing data and write-ups of other technicians for accuracy and completeness.
- Coordinating 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.
- Assists in the daily management of QC laboratory supplies and raw materials.
- Maintain instrument logs.
- Daily and weekly maintenance of instruments per SOP.
- Contributes to preparation and updating of QC standard operating procedures.
- Maintains meticulous documentation of all Quality Control records.
- Maintains lab housekeeping, organization, and inventory supply.
- Performs 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 and safe laboratory practices
- 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
TriLink BioTechnologies, a Maravai LifeSciences company, is a global leader in nucleic acid and mRNA solutions with over 29 years of experience since its founding in 1996. The company specializes in providing comprehensive CDMO services, high-quality readymade and custom materials, and innovative technologies including its patented CleanCap® mRNA capping technology. TriLink delivers unrivaled chemical and biological expertise to pharmaceutical leaders, biotech disruptors, and world governments, supporting critical applications from COVID-19 vaccine development to innovative treatments in oncology, infectious diseases, cardiology, and neurological disorders. Operating from its 118,000 sq ft facility in San Diego, California, TriLink offers scalable manufacturing capabilities, GMP-grade production, and extensive analytical services for mRNA characterization. The company's portfolio includes IVT kits, modified nucleotides, catalog RNAs, and custom oligonucleotide synthesis, serving both research and clinical development needs across the life sciences industry.