Senior Specialist QA & PMS

Work Flexibility: Hybrid or Onsite We are looking for a QA & PMS Specialist to support the implementation and maintenance of Quality Assurance and Post Market Surveillance activities across our MENA organization. What you will do: - Executing Quality Assurance (QA) and Post Market Surveillance (PMS) activities in line with local, regional, and corporate procedures and requirements. - Supporting the implementation and maintenance of the local Quality Management System (QMS) to ensure ongoing regulatory compliance. - Coordinating product safety reporting activities and supporting communications with relevant stakeholders, including healthcare professionals, distributors, and regulatory authorities. - Supporting the management of quality events, including non-conformances (NCs), corrective and preventive actions (CAPAs), and follow-up activities. - Assisting in the development, update, and implementation of quality procedures, work instructions, and SOPs. - Participating in internal and external audits and supporting inspection readiness activities. - Delivering quality and compliance training to employees and supporting onboarding of new team members. - Working cross-functionally to ensure quality requirements are effectively integrated into business processes. - Supporting the implementation of regional or global quality system changes within the local organization. - Monitoring, collecting, and reporting QA and PMS metrics and supporting continuous improvement initiatives. - Promoting a culture of quality and compliance across the organization. - Collaborating with EEMEA and global RAQA teams to support business and regulatory objectives. What you need: Required: - Bachelor’s degree in Engineering, Life Sciences, Healthcare, or a related field. - 1-3 years of experience in Quality Assurance, Regulatory Affairs, Post Market Surveillance, or a related healthcare or medical device environment. - Knowledge of Quality Management Systems and regulatory compliance principles. - Strong organizational, communication, and problem-solving skills. - Proficiency in Microsoft Office applications. - Fluency in English. Preferred: - Experience within the medical device, pharmaceutical, or healthcare industry. - Familiarity with NC, CAPA, complaint handling, or PMS processes. - Knowledge of ISO 13485, MDR, SFDA, or other applicable quality and regulatory requirements. - Arabic language skills are an advantage. Travel Percentage: 10%

Bachelor’s degree in Engineering, Life Sciences, Healthcare, or a related field. 1-3 years of experience in Quality Assurance, Regulatory Affairs, Post Market Surveillance, or a related healthcare or medical device environment. Knowledge of Quality Management Systems and regulatory compliance principles. Strong organizational, communication, and problem-solving skills. Proficiency in Microsoft Office applications. Fluency in English. Preferred: experience within the medical device, pharmaceutical, or healthcare industry; familiarity with NC, CAPA, complaint handling, or PMS processes; knowledge of ISO 13485, MDR, SFDA, or other applicable quality and regulatory requirements; Arabic language skills are an advantage.