Clinical FSP Quality Manager

IQVIA; Zaventem; Hybride; EUR 70 000 - 100 000; Plein temps

Résumé du poste

IQVIA is seeking an experienced QA professional to support global quality plans and GCP compliance across designated units. You will work with regional teams to ensure adherence to SOPs, ICH guidelines, and regulatory standards, driving continuous quality improvements.

The role requires 3+ years in clinical quality/GCP and 5+ years in medical devices or related fields, with strong ISO 14155 and audit experience. Hybrid work from Brussels is offered.

Qualifications

• This is a hybrid position with Brussels office 2–3 times per week.
• Minimum 3 years in a clinical quality/GCP compliance role.
• Minimum 5 years in medical device, clinical research, or related industry; strong ICH GCP and ISO 14155 knowledge.
• GCP audit experience is strongly preferred.

Responsabilités

• Adopt and implement the global Quality Management Plan within the assignment scope; plan and execute QA activities.
• Support risk identification/assessment and corrective/preventive actions; guide improvements.
• Provide advice on GCP compliance to teams and stakeholders.
• Collaborate to develop Delivery Unit/Sponsor quality plans and risk programs.
• Assist during audits and regulatory inspections as needed.

Connaissances

GCP compliance

Quality management

Regulatory knowledge

Auditing

Stakeholder collaboration

Description du poste

Job Overview

This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s), functional teams, and other stakeholders in a joint effort to clearly define the global Quality Plan, carry out, and adopt the plan according to the specific needs defined by the scope of assignment, assist staff in improving compliance with relevant International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), Key Performance Indicators (KPIs), applicable regulatory requirements, and guidelines.

Job Overview

This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s), functional teams, and other stakeholders in a joint effort to clearly define the global Quality Plan, carry out, and adopt the plan according to the specific needs defined by the scope of assignment, assist staff in improving compliance with relevant International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), Key Performance Indicators (KPIs), applicable regulatory requirements, and guidelines.

Essential Functions

• Adopt and implement the global Quality Management Plan within the scope of the assignment, this will include: Planning and executing the Quality Management activities. Risk identification and assessment through data review and quality control processes. Providing support in risk mitigation, in planning corrective/preventive actions, and guidance for improvement. Supporting the assigned business line management and staff to enhance effectiveness.;
• Cooperate closely with the relevant business and other stakeholders, support maintaining focus on quality in project delivery.
• Contribute to the development and implementation of a Delivery Unit/Sponsor specific Quality Management plan and Risk Management Program, monitor the implementation and delivery.
• Provide advice and support to teams within the assigned business line and other key stakeholders on all aspects of Good Clinical Practice (GCP) compliance.
• Work in close cooperation with teams to manage non-compliance, quality issues, support in planning corrective/preventive actions, as applicable according to Standard Operating Procedures (SOPs.);

Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.

• Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.
• Work closely with Quality Assurance and assigned business staff in case of suspected misconduct, as required by the applicable SOPs.
• May provide assistance during audits and regulatory inspections to the teams to the extent agreed with the business lines, as required by the applicable SOPs.
• Act as the primary contact for Quality Assurance on quality matters – on the level of the assignment, attend meetings/teleconferences.
• Prepare periodic reports to business lines on quality related matters, risk assessments and specific quality improvement initiatives.
• Upon agreement with the line manager: Perform any other reasonable tasks as required by the role.

Qualifications

• This is a hybrid position with a requirement to be at our office in Brussels 2-3 times/week.
• Have minimum of 3 years in a clinical quality/GCP compliance role
• Minimum of 5yrs experience in medical device, clinical research, or related industry- must have strong understanding of ICH GCP and know ISO 14155
• GCP audit experience is strongly preferred
• Knowledge of National and International Regulations and Drug Development processes.
• Knowledge of Clinical Research Organization (CRO) or Pharmaceutical industry operations.
• Excellent problem solving skills.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers.
• Fluent in English.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.