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Qualification/Validation Corporate Manager - Job Opportunity at Barrington James

Loiré, France
Full-time
Senior
Posted: April 6, 2025
Hybrid
EUR 70,000 - 90,000 per year based on French pharmaceutical industry standards and senior management level

Benefits

Hybrid work arrangement providing flexibility and work-life balance
Professional development opportunities in pharmaceutical validation
Exposure to cutting-edge industry practices and regulatory frameworks

Key Responsibilities

Strategic leadership of validation/qualification programs across corporate operations
Development and implementation of comprehensive validation strategies aligned with regulatory requirements
Cross-functional leadership and stakeholder management to ensure business objective alignment
Quality system oversight and documentation approval authority
Regulatory compliance management and industry standard implementation

Requirements

Education

Master's degree (Bac+5) in Quality, Quality Engineering, or Industrial Pharmacy

Experience

5 years minimum in quality within an industrial site

Required Skills

Strong interpersonal skills Proactivity Proficiency in Microsoft Office Suite Deep knowledge of GMP Quality standards expertise (ISO) Cross-functional team collaboration Documentation review and approval Regulatory compliance management
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Industry Trends

Increasing regulatory scrutiny in pharmaceutical manufacturing is driving higher demand for validation expertise Digital transformation in quality management systems is requiring broader technical competencies Growing focus on risk-based validation approaches aligned with FDA and EMA expectations

Role Significance

Typically leads a team of 5-8 validation specialists with matrix management of cross-functional teams
Senior management position with significant influence on quality systems and regulatory compliance

Key Projects

Implementation of site-wide validation master plans Qualification of new manufacturing facilities and equipment Development of risk-based validation strategies Regulatory inspection preparation and management

Success Factors

Strong technical expertise combined with strategic business acumen Ability to influence and align multiple stakeholders Deep understanding of regulatory trends and implementation strategies Effective communication skills across all organizational levels

Market Demand

High demand due to expanding pharmaceutical manufacturing sector and increased regulatory requirements in Europe

Important Skills

Critical Skills

GMP and quality systems expertise essential for ensuring regulatory compliance Strategic planning capabilities crucial for developing effective validation programs Stakeholder management skills vital for cross-functional success

Beneficial Skills

Project management methodologies Quality risk management tools Digital quality management systems Change management expertise

Unique Aspects

Role combines technical expertise with strategic business impact
Opportunity to shape validation practices in growing pharmaceutical operations
Position offers significant exposure to senior management and regulatory authorities

Career Growth

2-4 years in role before advancement, depending on business growth and organizational structure

Potential Next Roles

Quality Director Head of Technical Operations Site Quality Head Global Validation Director

Company Overview

Barrington James

Barrington James is a specialized life sciences recruitment firm with strong connections in the pharmaceutical and biotechnology sectors

Mid-sized recruitment specialist with established presence in European pharmaceutical recruitment
Strategic location in French pharmaceutical manufacturing region
Professional services environment with focus on pharmaceutical industry expertise and client relationships
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