automationcybersecurityplcgmpscadaoperational technologydisaster recoverycomputer system validation
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чёткая ответственность за регулируемые OT-системы в крупной компании из сферы наук о жизни даёт ценный специализированный опыт, но зарплата не указана, а работа предполагает присутствие на площадке.
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Зарплата не указанаАктуальные технологииПонятные задачиНауки о жизни
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
OT Engineer (Pharmaceutical Manufacturing/Automation): Designing, implementing, and maintaining OT systems for a regulated pharmaceutical oral solid dose manufacturing site with an accent on PLCs, SCADA, laboratory automation, cybersecurity, and GMP compliance. Focus on leading equipment integrations, validating systems under 21 CFR Part 11 and GAMP 5, testing disaster recovery, and troubleshooting complex automation and network issues.
Location: US - Tampa, FL
Company
hirify.global is a global life sciences company developing products and services for pharmaceutical and other life sciences applications.
What you will do
Manage the lifecycle, architecture, configuration, documentation, and compliance of OT systems including PLCs, HMIs, SCADA, BAS/BMS, LIMS, and LMS.
Maintain validated backups and perform restoration testing and disaster recovery activities across OT platforms.
Lead OT scope for equipment installations and upgrades, including FAT, SAT, commissioning, validation, and system integration with Engineering and IT.
Integrate laboratory instruments with OT infrastructure and troubleshoot automated laboratory workflows.
Provide advanced troubleshooting for automation faults and network issues in collaboration with Engineering, Quality Control, Maintenance, and IT.
Implement OT cybersecurity controls, manage user access and patching, support audits, author SOPs and validation documents, and contribute to automation optimization and digital transformation.
Requirements
Bachelor's degree.
At least 5 years of relevant experience.
Experience with OT systems such as PLCs, HMIs, SCADA, BAS/BMS, data historians, LIMS, LMS, and automation interfaces.
Knowledge of system reliability, cybersecurity, user administration, backup and recovery, and network troubleshooting.
Experience supporting Computer System Validation in alignment with 21 CFR Part 11 and GAMP 5.
Nice to have
Pharmaceutical or GMP experience.
Culture & Benefits
Full-time employment at a global life sciences organization.
Work focused on improving lives through pharmaceutical and life sciences products and services.
Ethical, respectful, and environmentally responsible working principles.
Equal opportunity employment.
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