Senior Specialist QA & PMS

Work Flexibility: Hybrid or OnsiteWe are looking for a QA & PMS Specialist to support the implementation and maintenance of Quality Assurance and Post Market Surveillance activities across the KSA 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%