Manager, Medical Devices

at  Jubilant DraxImage Inc

Montréal, QC, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate20 Nov, 2024Not Specified23 Aug, 2024N/AGood communication skillsNoNo
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Description:

sEnglish version below
Êtes-vous prêt à rejoindre une organisation qui offre un environnement dynamique et axé sur le client ?
Rejoignez-nous chez Jubilant Radiopharma, où nous combinons une expertise clinique mondiale avec un réseau pharmaceutique de premier plan pour soutenir nos clients et faire progresser la pratique de la médecine nucléaire. En tant que société pharmaceutique leader du secteur, nous sommes spécialisés dans le développement, la fabrication et la distribution d’agents diagnostiques et thérapeutiques de haute qualité. Notre mission est d’améliorer la vie grâce à la médecine nucléaire à l’échelle mondiale.
Nous avons une opportunité passionnante pour un chef, dispositifs médicaux, passionné par le fait de faire une différence dans la vie des patients.

WE OFFER YOU:

  • A career, not just a job!
  • Career growth and development opportunities
  • Supportive work culture
  • Competitive base salary
  • Annual bonus
  • Medical, dental and vision
  • RSP matching
  • Paid Time Off and paid holidays
  • Short and long-term disability coverage
    Are you passionate about driving innovation in medical devices? Do you thrive in a dynamic environment where your technical expertise can make a real impact? Jubilant Radiopharmaceuticals is looking for a Manager, Medical Devices to lead our cutting-edge projects and ensure the highest standards in medical device software development.

Responsibilities:

  • Drive hardware and software development for medical devices and related tools.
  • Lead software architecture and design activities, making critical technical decisions.
  • Collaborate closely with Installation & Training, Sales & Marketing, Program Management, Engineering, Regulatory, and Quality teams.
  • Manage an internal team and oversee activities for software development.
  • Ensure compliance with ISO13485, ISO14971, and IEC62304 standards.
  • Perform risk analysis, manage software change controls, and lead software verification and validation activities.
  • Support mechanical and electrical design activities and integrate hardware systems with software.
  • Oversee product change control processes to ensure products meet all specified requirements.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

Graduate

Proficient

1

Montréal, QC, Canada