Senior Specialist QA & PMS

PowerToFly; Riyadh; On-site; SAR 180,000 - 300,000; Full time

Job summary

Stryker is a global leader in medical technologies, seeking a QA & PMS Specialist to support Quality Assurance and Post Market Surveillance across the MENA region. The role ensures regulatory alignment, QMS maintenance, and effective collaboration with healthcare professionals, distributors, and regulators in Riyadh.

Responsibilities include managing NCs/CAPAs, audits, and training, while promoting a culture of quality and compliance across the organization.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, Healthcare, or related field.
• 1–3 years in QA, Regulatory Affairs, PMS, or related healthcare environment.
• Knowledge of Quality Management Systems and regulatory compliance.
• Strong organizational, communication, and problem-solving skills.
• Proficiency with Microsoft Office applications.
• Fluency in English.

Responsibilities

• Execute QA and PMS activities per local, regional, and corporate procedures.
• Support the local QMS implementation and regulatory compliance.
• Coordinate product safety reporting with healthcare professionals, distributors, and regulators.
• Support management of quality events, non-conformances, CAPAs, and follow-ups.
• Assist in developing and updating quality procedures, work instructions, and SOPs.
• Participate in audits and inspection readiness activities.
• Deliver quality and compliance training and onboard new team members.
• Collaborate cross-functionally to embed quality requirements into processes.
• Support regional/global QA system changes within the local organization.
• Monitor and report QA/PMS metrics and drive continuous improvement.
• Promote culture of quality and compliance.
• Collaborate with EEMEA and global RA/QA teams.

Skills

Quality Assurance

Regulatory Affairs

Post Market Surveillance

Communication

Problem-solving

Education

Bachelor’s degree in Engineering, Life Sciences, Healthcare, or related field

Tools

Microsoft Office

Job description

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.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.