# Senior Specialist QA & PMS — Stryker

Canonical: https://jobxdubai.com/jobs/r563967-senior-specialist-qa-pms
Location: Riyadh, Saudi Arabia
Type: full_time · Level: senior
Monthly salary: AED 17,640 to 25,480 per month (estimated, not employer-stated) (UAE salaries are tax-free)
Posted: 2026-09-11
Apply: https://stryker.wd1.myworkdayjobs.com/StrykerCareers/job/Riyadh-Riyadh-Offices-Zone/Senior-Specialist-QA---PMS_R563967

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## Description

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%

## Requirements

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.

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