About this role
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%