More jobs:
Quality Assurance Specialist
Job in
Riyadh, Riyadh Region, Saudi Arabia
Listed on 2026-05-02
Listing for:
Vitrolife Group
Full Time
position Listed on 2026-05-02
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
Quality Assurance Specialist – Riyadh
As a Quality Assurance Specialist, you will play a key role in driving compliance, enabling safe and effective services, and embedding a proactive quality culture – working closely with local teams and regional quality leadership.
Drive Quality Operations & Compliance- Oversee day-to-day quality activities and ensure adherence to local and regional requirements
- Maintain accurate quality records and actively participate in quality management forums
- Ensure compliance with MOH, SFDA, CBAHI, and other applicable regulations
- Manage document control processes to ensure procedures are current, compliant, and accessible
- Support implementation and updates of local and global procedures
- Contribute to continuous improvement of QMS processes
- Plan and conduct internal audits; manage findings and CAPA implementation
- Support external audits and regulatory inspections
- Lead local risk assessments and foster a proactive risk‑management culture
- Investigate deviations and ensure effective CAPA closure
- Monitor KPIs, incidents, and nonconformities
- Identify trends and escalates critical insights to Regional Quality Management
- Monitor regulatory changes and ensure timely implementation
- Support licensing, certifications, and renewals
- Ensure quality alignment in new or modified services
- Train and support staff on quality and regulatory requirements
- Evaluate external critical suppliers/service provider and referral laboratories to ensure compliance
- Contribute to regional and global quality initiatives and harmonization efforts
- Bachelor’s degree in Laboratory Sciences, Biomedical Sciences, or related field
- SCFHS license (preferred)
- Certification in Quality Assurance or Regulatory Affairs is a plus
- 3–4 years in a similar QA/regulatory role
- Experience with in laboratory or medical environment
- Strong knowledge of MOH and SFDA regulations (required)
- CBAHI standards (required)
- ISO 15189 and CAP accreditation (preferred)
- Strong understanding of QMS, audits, and documentation
- Experience with QMS/LIS systems
- Excellent problem‑solving and organizational skills
- Strong communication and collaboration abilities
- Fluent in Arabic and English (written and spoken)
- A proactive mindset – you don’t wait for issues, you prevent them
- The ability to translate regulations into practical, working processes
- Confidence to challenge, improve, and influence
- A strong sense of ownership and accountability
- Be part of an organization where quality is central to patient impact
- Work in a collaborative regional and global environment
- Contribute to high‑standard laboratory services and continuous improvement
- Grow within a culture that values expertise, structure, and innovation
- Preference will be given to Saudi Nationals
Structured, analytical, and proactive quality professional who thrives in regulated environments and enjoys collaborating across teams.
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