JobCubby JobCubby
Sign up
Stryker

Senior Specialist QA & PMS

Stryker Riyadh, Riyadh Region, Saudi Arabia

Medical Equipment Manufacturing · 10,001+ employees

5 d ago
qa Mid (2-5 yrs) Full-time Saudi Arabia
Create a free account to apply — email only, no card. You can also save this posting or score it against your profile with AI.

About the role

The Senior Specialist will execute Quality Assurance and Post Market Surveillance activities while maintaining the local Quality Management System to ensure regulatory compliance. They will also coordinate product safety reporting, manage quality events like CAPAs, and support internal and external audits.

What they look for

Quality Assurance Post Market Surveillance Regulatory Compliance Quality Management Systems CAPA Non-conformances Complaint Handling Internal Auditing Regulatory Affairs Medical Device Regulations ISO 13485 SOP Development Data Analysis Stakeholder Management Training Delivery Microsoft Office

Requirements

Candidates must hold a bachelor's degree in Engineering, Life Sciences, or Healthcare with 1-3 years of relevant experience in quality or regulatory environments. Proficiency in regulatory compliance principles and strong organizational skills are required, with knowledge of medical device standards being preferred.

Full 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%

Similar roles