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3 дня назад

Senior Automation Engineer (MedTech)

79 000 - 120 700$
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
Senior Automation Engineer (MedTech): Supporting and implementing validated manufacturing automation systems, interfaces, and execution-system code for a regulated healthcare facility with an accent on process control, compliance, and system lifecycle management. Focus on leading complex projects, performing validation and risk assessments, and applying predictive maintenance, advanced process control, and digital visualization.

Location: Malvern, Pennsylvania, United States of America

Salary: $79,000–$120,700 per year

Company

Johnson & Johnson MedTech develops healthcare and medical technology solutions focused on preventing, treating, and curing disease.

What you will do

  • Support and configure ISA-95 level 1 and 2 manufacturing automation systems, interfaces, and level 3 recipe content.
  • Implement or lead execution-system code changes and maintain compliance with site, global, and regulatory standards.
  • Write and perform validation protocols, lead risk assessments, support investigations, and participate in GMP audits and inspections.
  • Define project scope, coordinate resources, and track cost, quality, and schedule for project execution.
  • Represent the automation team as the business unit lead for the site’s large-scale development operations area.
  • Help implement predictive maintenance, multivariable analysis, advanced process control, and digital visualization tools.

Requirements

  • Bachelor’s degree or equivalent in engineering, industrial automation, information technology, or a related engineering field.
  • At least 2 years of experience in automation and a related position in a GxP-regulated environment.
  • Experience with process control systems, including Allen Bradley PLC.
  • Strong written and verbal communication, decision-making, problem-solving, and strategic change-leadership skills.
  • Ability to collaborate with Quality, IT, Lab Systems, Procurement, and other functional groups.

Nice to have

  • Knowledge of cGMPs and FDA regulations.
  • Experience with DeltaV, Ignition, Wonderware, or Desigo.
  • Lean or Six Sigma training or certification.
  • Experience with OSI PI historians, technology validation, design of experiments, and statistical analysis.

Culture & Benefits

  • Full-time employment within an inclusive and diverse work environment.
  • Vacation, sick time, holiday pay, personal and family time, and parental leave.
  • Caregiver, volunteer, military spouse, and condolence leave programs.
  • Accommodation support is available during the interview process for applicants with disabilities.

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