11 дней назад
Senior Automation Engineer (IOT)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Automation Engineer (IOT) (AspenTech IP.21/GMP): Maintaining and integrating the site Historian platform with plant automation, MES, SCADA, and manufacturing equipment in a biopharmaceutical facility with an accent on validated data acquisition, system reliability, and data integrity. Focus on Computer System Validation, industrial connectivity, cybersecurity, audit readiness, and supporting automation projects up to €5 million.
Location: Singapore
Company
is advancing biopharmaceutical manufacturing through its Modulus program, which develops flexible, scalable, and digitally enabled facilities for vaccines and Specialty Care biologics.
What you will do
- Serve as the site Subject Matter Expert for the plant Historian platform and maintain its availability, reliability, performance, and GMP compliance.
- Manage data connectivity between the Historian and MES, DeltaV, SCADA, benchtop equipment, and other manufacturing systems.
- Configure and support AspenTech IP.21 Historian, including Batch Extractor and SQL+.
- Lead Computer System Validation activities, qualification testing, system reviews, audit-trail reviews, and maintenance of validated systems.
- Develop SOPs and technical documentation covering operations, maintenance, backup and recovery, access management, and data retention.
- Support Tier 3 automation and digital transformation projects up to €5 million, including assessments, integrations, design reviews, and implementation.
Requirements
- Bachelor’s or Master’s degree in engineering, preferably chemical, electrical and electronic, instrumentation, industrial systems, pharmaceutical, or a related discipline.
- Industry experience in biopharmaceutical, biotechnology, pharmaceutical, or API manufacturing.
- Hands-on experience with AspenTech IP.21 Historian, Batch Extractor, and SQL+.
- Experience with ODBC, OPC UA, OPC DA, Profinet, manufacturing networks, virtualization, and industrial cybersecurity.
- Experience with CSV in regulated GMP environments, GxP compliance, Data Integrity, and pharmaceutical quality requirements.
- Ability to lead automation initiatives, coordinate system integrators, troubleshoot complex issues, and prepare GMP documentation.
Nice to have
- Experience with Manufacturing Execution Systems.
- Experience participating in global engineering or automation communities of practice.
Culture & Benefits
- Full-time employment in a fast-paced manufacturing environment.
- Cross-functional collaboration with Digital, Automation, IT, Manufacturing, Engineering, and external integrators.
- Participation in a global Community of Practice focused on harmonizing engineering and automation standards.
- Equal-opportunity workplace committed to diversity, equity, and inclusion.
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