مدير التنظيم والامتثال
Paxeramed Corp
نشرت قبل أكثر من 30 يومًا
أرسل لي وظائف مثل هذه
الجنسية
أي جنسية
جنس
غير مذكور
عدد الشواغر
1 عدد الشواغر
الوصف الوظيفي
الأدوار والمسؤوليات
1. Compliance Management
- Oversee all aspects of compliance with regulatory requirements, industry standards, and internal policies.
- Lead efforts to obtain and maintain certifications (e.g., ISO 9001,ISO 27000, ISO 13485, FDA , MDR, and other relevant quality/compliance standards).
- Ensure ongoing adherence to all applicable regulations, proactively identifying and addressing areas for improvement.
- Review, update, and maintain all regulatory files and documentation, ensuring timely submissions and filings.
- Monitor and interpret changes in laws, regulations, and industry standards; advise management on compliance implications.
2. Quality Assurance
- Implement and manage the company s Quality Management Systems (QMS).
- Collaborate with operations, product, and other teams to ensure products, services, and processes meet compliance and quality benchmarks.
- Conduct regular internal audits and assessments to evaluate compliance and certification readiness.
- Drive continuous improvement in quality processes through monitoring, feedback, and corrective action.
3. Risk Management & Reporting
- Develop and implement a risk management strategy to address potential non-compliance or quality issues.
- Maintain a compliance and certification risk register, ensuring risks are documented and mitigated.
- Monitor and report on the company s compliance status, providing regular updates to senior leadership.
- Investigate and resolve compliance-related issues or incidents, ensuring thorough root-cause analysis and preventive measures.
4. Collaboration & Leadership
- Partner with operations, product, and cross-functional teams to embed compliance into daily workflows.
- Act as the primary liaison for regulatory bodies, certification auditors, and external inspections.
- Provide training, awareness programs, and guidance to employees on compliance standards, policies, and regulatory requirements.
- Foster a culture of integrity, accountability, and continuous learning across the organization.
5. Process Improvement
- Lead continuous improvement initiatives to streamline compliance and certification processes.
- Enhance efficiency by automating and simplifying compliance workflows where possible.
- Stay updated on new regulations, compliance frameworks, and industry trends to anticipate and prepare for potential business impacts.
- Benchmark internal processes against best practices and recommend process optimizations.
الملف الشخصي المطلوب للمرشحين
Qualifications and Skills:
- Bachelor s degree in compliance, regulatory affairs, business administration, or related field.
- At least 3-5 years of experience in compliance, regulatory management, or quality assurance, ideally within the healthcare or software industry.
- Strong knowledge of industry regulations, quality standards (ISO), and compliance processes.
- Experience with obtaining ISO 9001,ISO 27000, ISO 13485, FDA , MDR.
- Excellent English Language.
- Excellent organizational, leadership, and communication skills.
- Ability to manage multiple projects and deadlines in a fast-paced environment.
القطاع المهني للشركة
- طب
- رعاية صحية
- تشخيص
- أجهزة طبية
المجال الوظيفي / القسم
- الجودة
- فحوصات
- ضمان الجودة
- التحكم بالجودة
- مفتش
الكلمات الرئيسية
- مدير التنظيم والامتثال
تنويه: نوكري غلف هو مجرد منصة لجمع الباحثين عن عمل وأصحاب العمل معا. وينصح المتقدمون بالبحث في حسن نية صاحب العمل المحتمل بشكل مستقل. نحن لا نؤيد أي طلبات لدفع الأموال وننصح بشدة ضد تبادل المعلومات الشخصية أو المصرفية ذات الصلة. نوصي أيضا زيارة نصائح أمنية للمزيد من المعلومات. إذا كنت تشك في أي احتيال أو سوء تصرف ، راسلنا عبر البريد الإلكتروني abuse@naukrigulf.com
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