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Текст:
Hirify AI/Оригинал
TL;DR
Compliance Director (Pharmaceutical Compliance): Leading compliance programs and complex initiatives in the pharmaceutical industry with an accent on regulatory guidance, audits, investigations, and compliance training. Focus on advising senior management, solving complex legal and operational problems, and developing strategic plans that improve compliance effectiveness and business operations.
Location: Shanghai, China
Company
hirify.global develops medicines and works to improve patient health and safety through regulated pharmaceutical operations.
What you will do
Ensure compliance with applicable laws, regulations, and internal policies, advising senior management on compliance matters.
Oversee compliance programs and initiatives, including leading or co-leading highly complex projects.
Develop mid-term plans and provide strategic guidance to business units.
Advise stakeholders, recommend courses of action, and influence management and senior staff decisions.
Independently solve complex problems, exercise judgment, and review colleagues’ work for effectiveness and quality.
Improve compliance and business operations through strategic planning, innovative solutions, audits, investigations, and training programs.
Requirements
Bachelor’s degree or higher.
10–15 years of compliance experience in the pharmaceutical industry is required; medical device industry experience may also be considered.
Business Partner or Center of Excellence (COE) experience is required.
Extensive knowledge of compliance laws and regulations, with the ability to manage complex compliance programs.
Strong analytical, problem-solving, written and verbal communication skills.
Experience with compliance audits and investigations.
Proficiency with compliance management software and tools.
Strong leadership and project management capabilities.
Ability to develop and implement effective compliance training programs.
Nice to have
Additional pharmaceutical industry experience.
Knowledge of international compliance regulations.
Advanced degree in law or a related field.
Experience working with regulatory agencies.
Success influencing senior management.
Ability to navigate complex legal and regulatory environments.
Strategic thinking, planning, interpersonal, relationship-building, organizational, and time-management skills.
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem-solving and productivity, with an understanding of responsible AI practices, risk management, and ethical use.
Culture & Benefits
Full-time employment in Shanghai, China.
Commitment to patient safety, regulatory excellence, compliance, and ethical business practices.
Equal opportunity employment in accordance with applicable legislation.
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