CHC Global Head of Audits and Inspections - Job Opportunity at Opella

Paris, France
Full-time
Executive
Posted: June 7, 2025
Hybrid
EUR 180,000 - 250,000 annually plus executive benefits package. This estimate reflects the executive nature of the role, extensive experience requirements, global scope of responsibilities, and Paris location premium. Senior quality leadership positions in major pharmaceutical companies typically command premium compensation due to their direct impact on regulatory compliance and business continuity.

Benefits

Challenging and purposeful work environment with empowerment to develop consumer brands with passion and creativity
Opportunity to be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best
Professional development opportunities to grow new skills in a global healthcare organization
Mission-driven work contributing to making self-care accessible for over half a billion consumers worldwide
International exposure working with global teams across 13 manufacturing sites and multiple markets
Association with a B Corp certified company demonstrating commitment to social and environmental responsibility

Key Responsibilities

Lead and strategically direct the CHC Global Quality Audit team encompassing all audit activities across the organization's global operations
Create, design, and implement comprehensive auditing systems for internal, external, and inspection readiness management that directly impact the company's right to manufacture and sell products
Provide executive leadership on critical audit activities for CHC sites, locations, and key third-party partners, ensuring compliance with global quality standards
Develop, direct, and approve annual audit plans with associated strategic planning and management reporting that drives organizational compliance outcomes
Provide strategic direction and operational support for CHC site regulatory inspections, ensuring readiness and successful outcomes with health authorities
Maintain executive-level interaction with the CHC Chief Quality Officer and Global Quality Senior Leadership team to ensure robust governance of audit findings and CAPA implementation
Collaborate with Internal Audit and Internal Control functions to identify and implement synergistic audit approaches that maximize organizational benefit
Create and establish CHC Global Quality Directives, Standards, Guidelines, and Procedures that shape organizational quality culture
Engage with regulatory authorities and external industry organizations to create leadership opportunities and strategic collaborations for CHC within the pharmaceutical industry

Requirements

Education

Minimum Bachelors degree in Pharmacy, Chemistry or related discipline. Masters/ PhD preferred

Experience

Minimum 15 Years experience in Quality management and pharmaceutical production with a good mix of technical, leadership and operational experience

Required Skills

Qualified Auditor Continuous improvement GxP and health-related regulations Quality risk analysis Quality risk management Quality systems Regulatory and company requirements, specifically pharmaceutical drug and nutraceuticals Regulations, e.g., drug law, GMP, Pharmacopeia, ICH Organization and communication skills networking capability leadership assertiveness skills

Certifications

Qualified Person status and advantage Qualified Auditor
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Industry Trends

The consumer healthcare and over-the-counter pharmaceutical market is experiencing unprecedented growth driven by increased consumer awareness of preventive healthcare and self-medication trends. This growth is creating significant demand for senior quality assurance professionals who can navigate complex global regulatory environments while ensuring product safety and compliance across multiple jurisdictions. Regulatory scrutiny in the pharmaceutical and consumer healthcare sectors has intensified globally, with health authorities implementing more stringent inspection protocols and quality requirements. This trend is driving organizations to invest heavily in audit and inspection readiness capabilities, making roles like this increasingly critical and well-compensated. The shift toward global supply chain management in pharmaceutical manufacturing has created complex quality oversight challenges, requiring senior professionals who can manage audit activities across diverse geographical regions, manufacturing partners, and regulatory frameworks. Companies are prioritizing executive-level positions that can provide strategic oversight of these multi-faceted quality operations.

Role Significance

Typically manages a global team of 15-25 quality audit professionals across multiple regions, with matrix management responsibilities for quality personnel at manufacturing sites and coordination with external audit firms and regulatory consultants.
This is a C-suite adjacent executive role with direct reporting relationships to the Chief Quality Officer and significant strategic influence over the organization's global quality operations. The position carries ultimate accountability for audit outcomes that directly impact the company's licensing and market access rights, indicating very high organizational importance and executive-level decision-making authority.

Key Projects

Implementation of comprehensive global audit management systems and digital quality platforms Leading major regulatory inspection preparation initiatives across multiple manufacturing sites Development and execution of supplier audit programs for key third-party manufacturers and CDMOs Strategic quality risk assessment projects that influence manufacturing location decisions and market entry strategies Cross-functional initiatives integrating quality audit outcomes with business continuity and supply chain optimization

Success Factors

Demonstrated ability to build and maintain strategic relationships with global regulatory authorities, as these relationships are critical for managing inspections and ensuring favorable regulatory outcomes that directly impact business operations Proven track record in leading large-scale organizational change initiatives, particularly in implementing new quality systems and audit processes across culturally diverse, geographically distributed teams Strong business acumen combined with deep technical expertise, enabling effective translation of regulatory requirements into practical business strategies and operational improvements Executive presence and communication skills necessary for presenting audit findings and quality strategies to board-level stakeholders and external regulatory authorities Cultural intelligence and adaptability required for managing quality standards across diverse international markets with varying regulatory frameworks and business practices

Market Demand

Very High - Executive-level quality assurance professionals with global audit expertise are in extremely high demand as pharmaceutical and consumer healthcare companies face increasing regulatory complexity and supply chain challenges.

Important Skills

Critical Skills

GxP regulatory expertise is absolutely essential as this role directly impacts the company's ability to maintain manufacturing licenses and market authorizations across global jurisdictions. Deep understanding of GMP, ICH guidelines, and regional regulatory variations determines success in managing inspection outcomes and maintaining compliance Global audit management capabilities are critical for establishing consistent quality standards across diverse manufacturing partners, internal sites, and supply chain components. The ability to design and implement comprehensive audit systems directly correlates with organizational risk management and business continuity Executive leadership and stakeholder management skills are crucial for success in this role, as the incumbent must influence quality outcomes across autonomous business units, negotiate with regulatory authorities, and present complex quality strategies to senior leadership and board members

Beneficial Skills

Digital quality system expertise and data analytics capabilities are increasingly valuable as pharmaceutical companies implement Industry 4.0 technologies and leverage real-time quality monitoring systems Supply chain risk management knowledge provides additional value given the increasing complexity of global pharmaceutical supply networks and the need for integrated quality oversight across multiple manufacturing partners Mergers and acquisitions experience would be highly beneficial given Opella's recent spin-out status and potential for future consolidation activities within the consumer healthcare sector

Unique Aspects

This role offers the rare opportunity to shape quality strategy for a major pharmaceutical spin-out during its critical independence phase, providing visibility into high-level strategic decisions and transformation initiatives
The position combines traditional pharmaceutical quality oversight with consumer healthcare and nutraceutical expertise, offering broader industry exposure than typical pharmaceutical quality roles
Direct interaction with global health authorities and industry organizations provides exceptional networking opportunities and influence within the pharmaceutical regulatory community
The role encompasses emerging areas such as digital health platforms and direct-to-consumer products, positioning the incumbent at the forefront of evolving consumer healthcare trends

Career Growth

3-5 years to Chief Quality Officer level, given the executive nature of current role and comprehensive global experience gained. Progression timeline may be accelerated based on successful management of major regulatory initiatives or expansion of organizational scope.

Potential Next Roles

Chief Quality Officer positions at major pharmaceutical or consumer healthcare companies Vice President of Global Quality or Regulatory Affairs roles with expanded portfolio responsibility Executive consulting positions specializing in pharmaceutical quality and regulatory strategy General Manager or Managing Director roles in pharmaceutical manufacturing operations

Company Overview

Opella

Opella represents a significant strategic spin-out from Sanofi's consumer healthcare division, positioned as the world's third-largest player in the over-the-counter and vitamins/supplements market. The company manages a portfolio of globally recognized brands including Allegra, Doliprane, and Dulcolax, with operations spanning 13 manufacturing sites and serving over 500 million consumers worldwide.

Opella holds a strong competitive position in the global consumer healthcare market, with significant market share in key therapeutic categories and a robust pipeline of established brands. The company's recent independence and B Corp certification demonstrate commitment to sustainable growth and social responsibility, positioning it favorably for continued market expansion.
The Paris headquarters location indicates this role will have substantial influence over European operations while maintaining global responsibility. Paris serves as a strategic hub for pharmaceutical regulation and provides access to key European health authorities, making this position critical for the company's regulatory strategy across major markets.
Opella's culture emphasizes challenger mentality and collaborative innovation, reflecting its position as a newly independent entity seeking to disrupt traditional consumer healthcare approaches. The organization promotes empowerment and accountability, with emphasis on sustainable impact and simplified consumer solutions.
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