Quality Control Manager – FSPx Client-Based in Paris Region
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Job Summary
Our FSPx department is expanding and we are looking for an experienced Quality Control Manager to join our team.
In this highly visible role you will act as a trusted quality partner to our Client ensuring that clinical trials are conducted in full compliance with GCP regulatory requirements and internal quality standards while actively contributing to process improvement and inspection readiness.
This position offers the opportunity to combine handson clinical expertise quality leadership and crossfunctional collaboration in an international environment.
This role is for upcoming future opportunities that may arise at Fortrea
Your role and Responsibilities:
As Quality Control Manager you will be responsible for (but not limited to):
- Lead the development monitoring coordination and execution of the annual countryspecific Quality Control (QC) plan
- Oversee the implementation and followup of QC activities ensuring alignment with Client expectations and regulatory standards
- Take ownership of Client Corrective and Preventive Actions (CAPA) arising from GCP audits and health authority inspections
- Manage and/or colead key Client quality initiatives contributing to inspection readiness and continuous improvement
- Act as a quality expert and advisor supporting clinical teams with GCP compliance risk mitigation and proactive quality oversight
- Ensure adherence to current Client processes and procedures while identifying opportunities to enhance and optimize ways of working
- Collaborate closely with crossfunctional stakeholders (Clinical Operations Quality Project Management Client representatives) in a matrix environment
Experience & qualifications
We are looking for a senior clinical research professional who brings:
- Minimum 68 years of clinical research monitoring experience
- Demonstrated experience leading crossfunctional teams or working in complex matrix environments
- Excellent site monitoring skills and a strong understanding of GCP requirements
- Excellent study site management capabilities with the ability to assess risk and quality proactively
- Proven experience working with audits inspections and CAPAs (direct responsibility preferred)
- Excellent verbal and written communication skills in French and English
- Strong analytical organizational and stakeholdermanagement skills
- A pragmatic solutionoriented mindset with a continuous improvement approach
- Willingness to travel up to 40% including overnight stays depending on project and country requirements
- Ability to drive and valid drivers license required
- Flexible working environment within an FSP model with close Client interaction
Why join us
- Be part of a highimpact FSPx environment working closely with a global pharmaceutical Client
- Play a key role in clinical quality compliance and inspection readiness
- Combine expert-level individual contribution with visible leadership and influence
- Work in an international collaborative and professional setting where quality truly matters
Learn more about our EEO & Accommodations request here.
Required Experience:
Manager
