Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У роли четкий объем задач senior-уровня, подробно описаны обязанности и понятна миссия в сфере medtech, но не указаны размер команды и соотношение аудита с консультационными задачами.
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Понятные задачиПольза для пациентовМеждународный масштаб
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Internal Auditor (Medical Device): Leading risk-based internal audits across global operations with an accent on governance, compliance, internal controls, SOX testing, and audit quality. Focus on planning and executing full audit lifecycles, identifying control gaps, developing remediation plans, and advising stakeholders on complex risk and process improvements.
Location: Hybrid, Guadalajara, Jalisco, Mexico
Company
hirify.global develops the Omnipod wearable, waterproof medical device platform to help patients live simpler and healthier lives.
What you will do
Lead and execute risk-based internal audit projects across global operations through planning, scoping, walkthroughs, testing, reporting, documentation, and follow-up.
Evaluate governance, risk management, compliance, operational processes, and internal controls, including applicable SOX testing.
Identify process, control, and regulatory compliance gaps and communicate findings to management and stakeholders.
Develop realistic remediation plans with the business, track audit findings, and incorporate follow-up procedures into future audits.
Support advisory services, emerging risk assessments, governance practices, and continuous improvement initiatives.
Build relationships with control owners and risk and compliance stakeholders, lead meetings, resolve problems, and provide recommendations for business and process improvement.
Requirements
Audit experience, including public accounting and/or corporate internal audit experience at a medium-to-large publicly traded company.
Competency and experience at the “Applied Knowledge” level within the IIA Competency Framework.
Working knowledge of professional standards, regulations, and frameworks relevant to internal audit.
Working knowledge of major business processes and compliance and risk issues in the medical device industry.
Strong analytical, critical-thinking, professional-skepticism, research, and problem-solving skills.
Strong written, verbal, and interpersonal communication skills, with the ability to challenge current practices and escalate concerns when warranted.
Ability to manage multiple concurrent audits, meet deadlines, work independently and collaboratively, and hold junior team members accountable.
Ability to build collaborative relationships with auditees, control owners, business partners, and risk and compliance stakeholders, and mentor junior team members.
Nice to have
BA/BS in Accounting or Finance.
Knowledge of the COSO internal control framework, Sarbanes-Oxley regulations, PCAOB standards and guidance related to internal controls, IIA Standards for the Professional Practice of Internal Auditing, and U.S. GAAP accounting standards.
Medical device experience, ESG and ERM exposure, and prior SAP or Optro (AuditBoard) experience.
Experience leading a team and providing developmental feedback.
Culture & Benefits
Hybrid work arrangement in Guadalajara, Jalisco, Mexico.
Work within a global operating environment and an Internal Audit function aligned with the IIA Global Internal Audit Standards.
Performance-driven culture guided by shared values and a focus on customer expectations.
Opportunity to contribute to innovative medical device technology intended to improve patients’ lives.
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