4 дня назад
Specialist, Quality Control (Laboratory Systems)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Specialist, Quality Control (Laboratory Systems) (Biotechnology): Supporting enterprise QC laboratory systems, master data, analytical templates, and electronic workflows across a global mRNA manufacturing network with an accent on GMP compliance, data integrity, and laboratory informatics. Focus on configuring LIMS, CDS, SoftMax Pro, and LES systems, troubleshooting complex workflows, and evaluating automation and AI-enabled QC capabilities.
Location: Madrid, Spain; hybrid 70/30 work model with 70% in-office collaboration.
Company
develops mRNA medicines and operates a global manufacturing and laboratory network supported by digital and analytical capabilities.
What you will do
- Support enterprise QC laboratory systems, including LabVantage LIMS, Chromeleon CDS, SoftMax Pro, Laboratory Execution Systems, and related applications.
- Provide Tier 1 technical support, troubleshoot user issues, document resolutions, and coordinate escalations with Digital and specialist teams.
- Configure and review laboratory master data, analytical templates, calculations, reports, LES worksheets, and electronic workflows.
- Support system enhancements, software upgrades, testing, deployment, validation documentation, change controls, deviations, and CAPAs.
- Maintain inspection-ready SOPs, work instructions, technical guidance, training materials, and controlled system documentation.
- Train QC users, drive global standardization, improve laboratory workflows, and evaluate automation and AI-enabled QC capabilities.
Requirements
- BS degree in science or a related scientific field.
- 3–5 years of experience in biotechnology or biopharmaceuticals, preferably in QC laboratories, laboratory systems, digital, or automation.
- Experience with laboratory informatics and enterprise systems such as LabVantage LIMS, Chromeleon CDS, SoftMax Pro, and/or LES.
- Knowledge of QC laboratory workflows, analytical methods, specifications, data review, master data, templates, calculations, and electronic worksheets.
- Experience in biopharmaceutical and GMP environments, with understanding of data integrity requirements.
- Proficiency in English is required for global collaboration.
Culture & Benefits
- In-person collaboration supported by a 70/30 office-based working model.
- Healthcare and voluntary benefit programs.
- Fitness, mindfulness, and mental health support.
- Family-building benefits, including fertility, adoption, and surrogacy support.
- Paid vacation, bank holidays, volunteer days, sabbatical, global 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 →
Похожие вакансии
4 дня назад
Tactical Communications Lab Test Engineer (Aerospace)
8 дней назад
Programm Quality Management Airbase Moron
4 дня назад
CAMO/MRO Mission Readiness Approval Manager
9 дней назад
HO Production Quality Space (Aerospace)
8 дней назад
Jig&Tools Quality Conformance Manager
10 дней назад