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Sr Engineer I, Automation (Syncade MES)

93 000 - 121 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Sr Engineer I, Automation (Syncade MES) (biopharmaceutical manufacturing automation): Administering and improving Syncade MES systems for electronic batch records, recipe configuration, and GMP manufacturing execution with an accent on system reliability, data integrity, and compliance. Focus on troubleshooting complex MES issues, leading deviation investigations and validation activities, and integrating Syncade with DeltaV, PI, LIMS, and enterprise systems.

Location: Research Triangle Park, North Carolina, United States

Salary: $93,000–$121,000 base salary per year

Company

hirify.global is a biotechnology company developing life-changing medicines through regulated biopharmaceutical manufacturing and research.

What you will do

  • Administer and serve as the subject matter expert for Syncade MES, including configuration, maintenance, troubleshooting, and lifecycle management.
  • Support electronic batch record workflows, recipe configuration, exception handling, and the infrastructure required for manufacturing execution.
  • Ensure system availability, performance, data integrity, user access, security roles, and audit trail compliance.
  • Lead root cause investigations, corrective and preventive actions, change controls, system updates, enhancements, and validation deliverables including IQ/OQ/PQ.
  • Support integrations and data flows between Syncade, DeltaV, PI, Infobatch, CMMS, Oracle, Veeva, and LIMS.
  • Provide technical support during manufacturing operations, including required off-hours support, and drive continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Engineering.
  • 5–8+ years of automation engineering experience in a regulated environment, preferably GMP.
  • At least 3 years of experience with Syncade/MES infrastructure, workflows, electronic batch record design, and manufacturing process support.
  • Strong understanding of GxP compliance, data integrity, and change control processes.
  • Ability to independently troubleshoot and resolve complex technical issues.
  • Experience supporting biopharmaceutical manufacturing systems and working with cross-functional teams.

Nice to have

  • Experience with Emerson DeltaV DCS integration and support.
  • Experience with AVEVA PI System for data collection and analytics.
  • Familiarity with Infobatch for batch reporting.
  • Participation in system upgrades, technology transfers, or manufacturing modernization initiatives.

Culture & Benefits

  • Full-time employment with medical, dental, vision, and life insurance.
  • Short- and long-term disability coverage, paid vacation, sick time, holidays, and parental leave.
  • 401(k) participation with company matching and an employee stock purchase plan.
  • Fitness and wellness programs, tuition reimbursement up to $10,000 per calendar year, and employee resource groups.
  • Short-term and long-term incentive opportunities, including cash bonuses and equity incentives.
  • Inclusive workplace focused on collaboration, learning, growth, and operational excellence.

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