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Roche
Roche
H1B vizos rėmėjasFarmacijos produktaiSveikatos draudimasSveikatos priežiūra
„Roche“ yra pasaulinė sveikatos priežiūros ir farmacijos įmonė, kurios tikslas – gerinti pacientų priežiūrą pasitelkiant mokslinius tyrimus ir plėtrą, skaitmenines inovacijas bei bendradarbiavimą. Daugiau nei 101 000 darbuotojų turinti įmonė sutelkia technologijų, gamybos, verslo strategijos ir kitų sveikatos priežiūros inovacijas palaikančių sričių kompetenciją. „Roche“ pabrėžia įvairovės, lygybės ir įtraukties svarbą tarptautinėse komandose bei siūlo karjeros galimybes patyrusiems specialistams, studentams ir absolventams, įskaitant galimybes, susijusias su įmonės veikla Vokietijoje, Austrijoje ir Šveicarijoje.
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Roche Regulatory Affairs Manager, IVD Instruments and Software

Lead regulatory submissions and strategy for Roche Diagnostics’ IVD instruments and software. Support product approvals across global markets, with a focus on Pathology and Digital Pathology.

USJungtinės ValstijosAZArizonaNJNaujasis Džersis
106 100 $ – 197 000 $ / metai
HibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųAtitiktis

Aprašymas

  • Coordinate regulatory projects for laboratory instruments, consumables, software, and integrated systems.
  • Support the Pathology and Digital Pathology portfolios within the Pathology Customer Area.
  • Oversee regulatory documents and submission dossiers for complex products and programs.
  • Develop and manage portions of global regulatory submissions and registration plans.
  • Apply US FDA requirements to IVD instruments, software, accessories, and system reagents.
  • Work with external leaders, customers, and other stakeholders.
  • Build external partnerships and apply stakeholder management practices.
  • Assist with audit preparation, execution, and follow-up.
  • Guide organizational adaptation to changing regulatory requirements.
  • Interpret regulator perspectives and apply regional regulatory strategies.
  • Develop strategies that address obstacles and support worldwide product approvals.
  • Collaborate with stakeholders to identify and deliver solutions.
  • Address challenges and opportunities with input from collaborators.
  • Build relationships that help shape Roche’s direction and its products.
  • Make independent decisions and proactively initiate work.
  • Demonstrate VAAC Leadership and agility while supporting an inclusive environment.
  • Unite colleagues around shared goals, resolve conflict, and improve team outcomes.

Reikalavimai

  • Bachelor’s or master’s degree in life sciences, data science, or a related field, or equivalent experience.
  • An advanced degree is preferred.
  • Experience in IVDs, medical devices, pharmaceuticals, or biopharmaceuticals with significant regulatory affairs experience: 3–5 years with a PhD, 5–7 years with a master’s degree, or 6–8 years with a bachelor’s degree, or equivalent.
  • Demonstrated experience with Daily Management and Continuous Improvement practices.
  • Knowledge of European, US, Chinese, and other international regulations.
  • Ability to interpret and implement quality standards is an advantage.
  • Ability to manage complex work and parts of global projects.
  • Experience with medical laboratory instruments, accessories, consumables, and software launch strategies in the US, EU, and other global markets is preferred.
  • Must live near Tucson, Indianapolis, Branchburg, or Carlsbad.
  • Relocation assistance is not available.

Privalumai

  • A discretionary annual bonus may be offered based on individual and company performance.
  • Benefits information is available at the provided link.
  • Roche is an equal opportunity employer.
  • Accommodation is available for applicants with disabilities during the online application process.

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