4 дня назад
Analyst, Quality Control, Microbiology
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Analyst, Quality Control, Microbiology (GMP/Microbiology): Performing environmental monitoring, water sampling, and microbiological testing for mRNA manufacturing with an accent on sterility, bioburden, endotoxin, and GMP quality systems. Focus on executing method transfers and qualifications, investigating deviations, maintaining data integrity, and supporting audits in a site-based QC laboratory.
Location: Oxford, England; site-based, full-time attendance required and not eligible for remote work
Company
develops mRNA-based therapeutics and vaccines through its mRNA science, delivery technology, and manufacturing platform.
What you will do
- Perform routine environmental monitoring and critical utility sampling in a GMP manufacturing facility.
- Analyze water samples for TOC, conductivity, bioburden, and endotoxin.
- Execute QC microbiology testing for sterility, bioburden, endotoxin, release, stability, and verification or validation samples.
- Support method transfers, qualifications, validations, assay troubleshooting, and collaboration with internal and external testing laboratories.
- Maintain laboratory systems, prepare and ship samples, perform equipment maintenance, and complete data entry in accordance with good documentation practices.
- Author and maintain quality records, including investigations, deviations, change controls, CAPAs, SOPs, protocols, and reports; support audits and junior staff.
Requirements
- BSc in a relevant scientific discipline.
- At least 2 years of Quality Control experience in a cGMP organization with a microbiology focus.
- Hands-on experience with microbiology techniques such as Vitek, isolator technology, bioburden, BET, and sterility testing.
- Working experience in a GMP environment and the ability to conduct investigations.
- Ability to collaborate in a cross-functional matrix environment and prioritize multiple tasks in a fast-paced setting.
- Ability and willingness to work full-time at the site in Oxford; remote work is not available.
Nice to have
- Working knowledge of current FDA, EU, and ICH guidelines and regulations.
Culture & Benefits
- In-person collaboration model with emphasis on innovation, teamwork, and direct mentorship.
- Healthcare and voluntary benefit programs.
- Fitness, mindfulness, and mental health support.
- Family-building benefits, including fertility, adoption, and surrogacy support.
- Paid time off, bank holidays, volunteer days, sabbatical, recharge days, and year-end shutdown.
- Savings and investment programs plus location-specific benefits.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →