Senior Quality Assurance Manager

ERGOMED

. Ensures continuous quality improvement through effective management and oversight of Audits and Inspections .

Posted 4/21/2026full-timeRemote • 🇶🇦 QatarSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensures continuous quality improvement through effective management and oversight of Audits and Inspections
Facilitates ongoing quality improvement measures through communication of audit & Inspection intelligence and compliance guidance/training
Leads, educates, mentors, and develops the team within the function to ensure their competence and confidence in developing to become subject matter experts
Ensures that reporting, review and analysis of Findings from Audits and Inspection and CAPAs is performed efficiently and in compliance with global regulations, legislation and PrimeVigilance requirements
Manages and maintains the electronic quality management system (EG-QMS) Audits module -CAPA Management
Performs periodic trending of Findings across the company, providing insights into the potential causes of trends to operational and quality management
Fosters a culture of quality within the organisation as led by members of the Quality Leadership Team
Participates in audits and inspections, including document request provision, front and back-room activities, and follow-up of audit and inspection findings and completion of client questionnaires and RFP/RFI
Acts as a Subject Matter Expert and client point-of-contact for Quality including attendance at operational and quality governance meetings
Collaborates and guides operational personnel to ensure effective root cause analysis and writing/delivery of appropriate CAPA Plans and develops and delivers training on these topics and other quality topics
Generates metrics on CAPA compliance
Assists in the development, maintenance and management of mechanisms that assure ongoing monitoring and compliance with all applicable laws and regulations including but not limited to EU GVP, US FDA CFRs, JMPA and ICH-E6
Procedural creation, management revision

Requirements

What you’ll need

A university degree in a healthcare discipline or equivalent scientific area
Substantial experience in pharmaceutical/biotechnology pharmacovigilance with a in depth understanding of GVP/GCP-related Quality Management and Assurance
Sound knowledge of international regulations related to Pharmacovigilance and Medical Information
Experience of participating in audits and inspections
Ability to lead, mentor, and develop teams
Excellent communication and facilitation skills within a global organization
Proactive and self-motivated with strong organizational and planning abilities
Excellent problem-solving and decision-making skills
Attention to detail and commitment to high standards
Ability to analyze data and prepare detailed reports
Knowledge of quality management principles and practices

Benefits

Comp & perks

Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly, supportive working environment
Opportunity to work with colleagues based all over the world, with English as the company language

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

quality managementCAPA managementdata analysisreport writingroot cause analysisauditsinspectionsGVPGCPpharmacovigilance

Soft Skills

leadershipmentoringcommunicationfacilitationorganizational skillsplanningproblem-solvingdecision-makingattention to detailproactive