11 часов назад
Automation Project Engineer
103 200 - 161 250$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Automation Project Engineer (GMP Manufacturing and SCADA): Designing, implementing, and maintaining automation and control systems for oligonucleotide therapeutics manufacturing facilities with an accent on plant control systems, data integrity, and regulatory compliance. Focus on leading automation upgrades and expansions, integrating Rockwell, SCADA, historian, and IT/OT systems, and supporting commissioning, qualification, and validation.
Location: US-CO-Boulder; work at GMP manufacturing facilities in Boulder and Frederick, Colorado. Occasional travel; day shift.
Salary: $103,200–$161,250 per year, plus eligibility for bonus, stock, and benefits.
Company
develops technologies and operates manufacturing facilities supporting the oligonucleotide therapeutics industry.
What you will do
- Design, implement, maintain, and start up automation and control systems for GMP manufacturing operations.
- Act as the technical lead for automation upgrades, plant expansions, integration design, and implementation.
- Manage contractors and consultants while coordinating with Engineering, Manufacturing, Quality Assurance, Validation, and IT.
- Define project scope, milestones, deliverables, budgets, and resource requirements.
- Maintain control-system lifecycle specifications, lead change controls, and ensure data integrity and 21 CFR Part 11 compliance.
- Support CQV activities, IT/OT network development, safety programs, and evaluation of new automation technologies.
Requirements
- Bachelor’s or master’s degree in electrical, mechanical, or chemical engineering, or equivalent education and experience.
- 4+ years of controls experience across assignments with increasing breadth and complexity.
- Project management experience and practical application of project fundamentals.
- Experience with Rockwell Automation products, GE Proficy iFix SCADA, Ignition, and ThinManager thin-client architecture.
- Familiarity with server and network architecture.
- Previous GMP or pharmaceutical manufacturing experience is highly desirable.
Culture & Benefits
- Full-time employment with a regular weekly schedule and no specified end date.
- Eligibility for bonus, stock, and benefits.
- Focus on safe work practices and adherence to safety protocols.
- Inclusive, merit-based workplace with accessibility support for candidates with disabilities.
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