3 часа назад
QC Associate - Temp (Molecular Biology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
QC Associate - Temp (Molecular Biology): Performing routine QC release testing, product review, and analytical laboratory activities for molecular biology products with an accent on validated methods, data integrity, and ISO 13485:2016 compliance. Focus on executing qPCR, NGS, electrophoresis, and spectroscopic testing, investigating OOS/OOT results, and maintaining reliable QC records and instruments.
Location: Onsite in Wilsonville, Oregon, USA; Monday-Friday, 8:00 am-5:30 pm PT. Shift, weekend, holiday, or on-call coverage may be required.
Company
develops biotechnology products supported by molecular biology and quality control laboratory operations.
What you will do
- Perform routine QC release testing, data review, and basic product release activities under direct supervision.
- Execute validated analytical methods, including qPCR, NanoDrop/Qubit measurements, fragment analysis, and basic NGS QC tasks.
- Inspect incoming raw materials and prepare disposition recommendations for senior QC approval.
- Support OOS and OOT investigations by gathering raw data, documenting findings, and escalating atypical results.
- Maintain QC records, instrument logs, reagents, standards, assay controls, and laboratory inventory.
- Perform environmental monitoring, water sampling, instrument maintenance, and continuous improvement activities as applicable.
Requirements
- BS in Biochemistry, Chemistry, Molecular Biology, or a related field.
- 0-2 years of industrial Operations/QC experience; internship, co-op, or relevant academic laboratory experience may substitute.
- Knowledge of molecular biology techniques, including PCR, cloning, and sequencing, plus analytical methods such as spectroscopy and gel electrophoresis.
- Basic laboratory skills, including pipetting, sample handling, and instrument operation; familiarity with LIMS.
- Working knowledge of Good Manufacturing Practices and Good Documentation Practices.
- Ability to work onsite in a laboratory, cleanroom, and manufacturing environment, including gowning and personal protective equipment requirements.
Nice to have
- Hands-on experience with automated liquid-handling or robotic systems.
- Experience with QC or QA operations in a regulated biotechnology or manufacturing environment.
Culture & Benefits
- Fast-paced, team-oriented, and collaborative QC environment.
- Work includes frequent standing, walking, repetitive pipetting, and lifting up to 25 lbs with or without reasonable accommodation.
- Operations follow ISO 13485:2016, internal SOPs, ALCOA+ data integrity principles, and 21 CFR Part 11 requirements.
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