Home Jobs Regulatory Affairs Manager M/F
Back to Jobs

Regulatory Affairs Manager M/F - Job Opportunity at Ceva Tiergesundheit GmbH

Beaucouzé, France
Full-time
Senior
Posted: July 3, 2025
Hybrid
EUR 65,000 - 85,000 per year based on the senior-level requirements, specialized veterinary regulatory expertise, and the company's position as a global leader in animal health. The salary range reflects the 5-10 years experience requirement and the strategic nature of the role involving cross-functional leadership and authority relationship management.

Benefits

Opportunity to work with a global leader in animal health industry providing significant career advancement potential
International work environment with collaboration across multiple countries and regulatory frameworks
Comprehensive professional development through interaction with R&D, manufacturing, Quality Control, Quality Assurance and Marketing teams
Disability-inclusive workplace with reasonable accommodations and commitment to diversity, equity and inclusion
Hybrid work arrangement with remote work flexibility from Angers-based position
Strategic role involvement in business risk management and regulatory compliance decisions

Key Responsibilities

Lead comprehensive regulatory lifecycle management for veterinary medicinal product portfolios, directly impacting business continuity and market access across multiple jurisdictions
Orchestrate cross-functional collaboration with R&D, manufacturing, Quality Control, Quality Assurance and Marketing teams to prepare technical registration files that drive new product launches
Manage strategic submission processes to local authorities and oversee complex regulatory procedures that determine market entry timelines
Provide executive-level advisory services on regulatory opportunities and risks, enabling business units to capitalize on growth opportunities and mitigate potential losses
Develop and maintain strategic relationships with regulatory authorities across assigned territories, positioning the company as a trusted partner in veterinary health
Execute proactive regulatory compliance monitoring against internal and external regulations, ensuring operational excellence and legal adherence
Lead business risk assessment and management activities related to product registration and manufacturing site authorizations

Requirements

Education

Degree in veterinary medicine or pharmacology or a master's degree in biology with additional training in regulatory affairs

Experience

5-10 years experience in the field of immunological veterinary medicinal products

Required Skills

Fluent in English Dynamic personality with affinity for challenges Interest in joining an international company
Advertisement
Ad Space

Sauge AI Market Intelligence

Industry Trends

The animal health industry is experiencing unprecedented growth driven by increasing pet ownership, expanding livestock production, and growing awareness of zoonotic diseases. Regulatory affairs professionals are becoming increasingly critical as companies navigate complex global regulatory landscapes while accelerating product development timelines. The 'One Health' approach is reshaping regulatory strategies, requiring professionals who can integrate human, animal, and environmental health considerations into regulatory frameworks. Digital transformation in regulatory affairs is revolutionizing how companies manage submissions, track compliance, and interact with authorities. This shift is creating demand for regulatory professionals who can leverage technology while maintaining deep expertise in traditional regulatory processes. Companies are investing heavily in regulatory technology platforms, creating opportunities for professionals who can bridge technical and regulatory expertise. Post-pandemic regulatory environments are emphasizing supply chain resilience and rapid response capabilities. Regulatory affairs managers are increasingly responsible for ensuring business continuity through diversified manufacturing authorizations and flexible regulatory strategies. The focus on veterinary medicinal products has intensified as the connection between animal and human health becomes more apparent in global health security discussions.

Role Significance

Typically manages a team of 3-5 regulatory specialists while collaborating with multiple cross-functional teams including R&D, manufacturing, quality assurance, and marketing. The role likely involves matrix management responsibilities and coordination of regulatory activities across multiple product lines and geographic regions.
Senior-level position with significant strategic impact, evidenced by the requirement for 5-10 years of specialized experience and responsibility for managing complex regulatory lifecycles. The role involves executive-level advisory functions and cross-functional leadership, indicating substantial organizational influence and decision-making authority.

Key Projects

Implementation of global regulatory harmonization initiatives across multiple jurisdictions Management of new product registration campaigns for innovative veterinary medicinal products Development of regulatory strategies for manufacturing site transfers and expansions Creation of regulatory compliance frameworks for emerging markets Leadership of regulatory due diligence activities for potential acquisitions or partnerships

Success Factors

Deep understanding of global veterinary regulatory frameworks and the ability to navigate complex multi-jurisdictional requirements while maintaining strategic business perspective Exceptional cross-functional collaboration skills enabling effective coordination between technical, commercial, and regulatory teams to achieve business objectives Strong relationship management capabilities for building productive partnerships with regulatory authorities and internal stakeholders Strategic risk assessment abilities to identify and mitigate regulatory risks while capitalizing on opportunities for business growth Adaptability to evolving regulatory landscapes and the ability to translate regulatory changes into actionable business strategies

Market Demand

High demand driven by the expanding animal health market, increasing regulatory complexity, and the critical nature of regulatory compliance in pharmaceutical industries. The specialized combination of veterinary medicine knowledge and regulatory affairs expertise creates a competitive talent market.

Important Skills

Critical Skills

Regulatory affairs expertise is absolutely fundamental as this role requires deep understanding of complex veterinary pharmaceutical regulations across multiple jurisdictions. The ability to navigate regulatory landscapes directly impacts product launch timelines and market access strategies, making this expertise essential for business success. Cross-functional collaboration skills are critical because the role requires coordination with R&D, manufacturing, quality assurance, and marketing teams. Success depends on the ability to align diverse stakeholder interests while maintaining regulatory compliance and business objectives. Strategic thinking and business acumen are essential for evaluating regulatory opportunities and risks, providing advisory services to business units, and contributing to growth strategies. The role requires the ability to translate regulatory requirements into business implications and recommendations.

Beneficial Skills

Digital regulatory technology proficiency would be highly valuable as the industry continues to embrace electronic submissions and regulatory information management systems Project management expertise would enhance the ability to coordinate complex registration activities and cross-functional initiatives Foreign language capabilities beyond English would be advantageous for direct communication with European regulatory authorities and international stakeholders Financial analysis skills would support business case development for regulatory strategies and investment decisions Change management expertise would be valuable for implementing new regulatory processes and managing organizational transitions

Unique Aspects

Specialized focus on veterinary medicinal products requiring unique regulatory expertise that combines pharmaceutical knowledge with veterinary medicine understanding
Integration of 'One Health' principles into regulatory strategy, reflecting the company's forward-thinking approach to interconnected health systems
Significant international scope with responsibility for multiple jurisdictions and regulatory frameworks
Direct involvement in strategic business risk management and growth opportunity identification
Hybrid work arrangement offering flexibility while maintaining collaborative team environment

Career Growth

Progression to director-level roles typically occurs within 3-5 years with demonstrated success in managing complex regulatory portfolios and teams. Executive-level positions may be achievable within 5-8 years with strong business acumen and strategic leadership capabilities.

Potential Next Roles

Global Regulatory Affairs Director overseeing multiple regional teams and strategic regulatory initiatives Head of Regulatory Affairs with P&L responsibility and executive team membership Vice President of Regulatory and Quality Affairs combining regulatory and quality management functions Chief Regulatory Officer position in smaller animal health companies Regulatory Affairs Consultant providing specialized expertise to multiple animal health organizations

Company Overview

Ceva Tiergesundheit GmbH

Ceva Animal Health is a global veterinary pharmaceutical company headquartered in France, specializing in the research, development, production, and marketing of veterinary medicines and vaccines. The company operates in over 40 countries and focuses on farm animals, companion animals, and wildlife health solutions. Ceva has established itself as a significant player in the animal health industry through strategic acquisitions and organic growth initiatives.

Ceva holds a strong position in the global animal health market, ranking among the top 10 animal health companies worldwide. The company has demonstrated consistent growth and maintains a diverse portfolio of innovative products across multiple therapeutic areas. Their commitment to the 'One Health' approach positions them well for future regulatory and market developments.
The position in Beaucouzé, France, places the role at the heart of Ceva's European operations, with significant influence over regulatory strategies across the EU market. This location provides access to key regulatory authorities and positions the role as a critical link between global regulatory strategy and European market execution.
Ceva emphasizes collaborative innovation and cross-functional teamwork, as evidenced by their commitment to diversity, equity, and inclusion initiatives. The company culture appears to value professional development and provides opportunities for international exposure and career advancement within a growing global organization.
Advertisement
Ad Space
Apply Now

Data Sources & Analysis Information

Job Listings Data

The job listings displayed on this platform are sourced through BrightData's comprehensive API, ensuring up-to-date and accurate job market information.

Sauge AI Market Intelligence

Our advanced AI system analyzes each job listing to provide valuable insights including:

  • Industry trends and market dynamics
  • Salary estimates and market demand analysis
  • Role significance and career growth potential
  • Critical success factors and key skills
  • Unique aspects of each position

This integration of reliable job data with AI-powered analysis helps provide you with comprehensive insights for making informed career decisions.