Quality Manager - Africa / Europe (full-time, remote)

Onqsa; United States; Remote; USD 80,000 - 100,000; Full time

Job summary

Join a leading healthcare research company as a Quality Manager, responsible for developing and maintaining a robust Quality Management System. This remote role involves ensuring compliance with global GxP standards and continuous improvement across processes. You'll work with a multicultural team, fostering a culture of respect and inclusion while managing audits and quality metrics.

Qualifications

• 2-5 years of experience in a GCP-regulated environment.
• At least 2 years conducting GCP audits.

Responsibilities

• Manage QMS processes ensuring compliance with regulatory standards.
• Conduct internal, site, and third-party audits.
• Develop and oversee quality metrics related to deviations and CAPA.

Skills

Analytical thinking

Collaboration

Problem-solving

Communication

Interpersonal skills

Organizational skills

Education

Bachelor’s or PhD in Life Sciences

Tools

Electronic document management systems

Audit management systems

Job description

Quality Manager - Africa / Europe (full-time, remote)

Join to apply for the Quality Manager - Africa / Europe (full-time, remote) role at OnQ Research - A P95 company

Job Purpose
The Quality Manager is responsible for developing, implementing, and maintaining a robust Quality Management System (QMS) in compliance with global and local GxP (good practices) regulatory requirements such as GCP, GEP, GVP, and ISO. This role ensures adherence to quality standards across processes, continuous improvement, and operational excellence.

Position Details
Permanent, Full-time, Remote

Responsibilities

• Manage assigned QMS processes ensuring compliance with regulatory standards;
• Develop and update Policies, SOPs, Guidance, and Work Instructions;
• Monitor and report training compliance, identify gaps, and implement corrective actions;
• Manage quality questionnaires and due diligence activities;
• Develop and oversee quality metrics related to deviations, CAPA, risks, and change controls;
• Conduct internal, site, and third-party audits, ensuring compliance and identifying improvements;
• Support external audits and inspections, including document preparation and hosting.

Candidate Requirements

• Bachelor’s or PhD in Life Sciences;
• 2-5 years of experience in a GCP-regulated environment;
• At least 2 years conducting GCP audits;
• Experience with quality questionnaires and due diligence;
• Ability to write and implement standards, process flowcharts, and RACI matrices;
• Experience with internal, third-party, and external audits;
• Knowledge of training management, risk management, deviations, CAPA, and change control;
• Proficiency with electronic document and audit management systems;
• Strong problem-solving and continuous improvement skills.

Skills

• Analytical thinking and collaboration skills;
• Autonomous problem-solving and process improvement mindset;
• Excellent communication, interpersonal, and organizational skills;
• Ability to work under pressure, remotely, and as part of a team;
• Client-focused with sensitivity to cross-cultural differences.

Why Join Us?

You will be part of a dynamic, multicultural team of nearly 300 professionals across over 20 countries, working remotely with flexible schedules. We foster a culture of respect, inclusion, and purpose-driven work in healthcare research.

Visit our website www.p-95.com to learn more and apply via our short form. The position remains open until filled.