At a Glance
- Tasks: Lead global quality audits and build a sustainable inspection readiness framework.
- Company: Dynamic organisation focused on dermatology with a diverse culture.
- Benefits: Hybrid work culture, competitive pay, bonuses, and global career opportunities.
- Other info: Cross-functional exposure and proactive problem-solving environment.
- Why this job: Make a real impact on regulatory compliance and audit governance.
- Qualifications: 10+ years in audit management within Pharma/Medical Devices.
The predicted salary is between 42750 - 52250 £ per year.
In this role you will lead global quality audits and build a sustainable inspection readiness framework to support regulatory inspections across EMEAC. You will develop and enhance auditing capabilities, monitor regulatory trends, and guide regions to strengthen compliance. The position offers cross-functional exposure within a growing, diverse organization focused on dermatology. You will impact audit governance, readiness, and the company’s regulatory posture.
Pay / Benefits
- hybrid work culture
- competitive compensation with bonus
- extended benefit package
- global career opportunities
- ownership from day one
Responsibilities
- Lead regionally managed quality audits (internal, external, supplier) across EMEAC with risk-based planning and timely closure
- Establish and govern a global inspection readiness framework ensuring preparedness for regulatory inspections
- Develop and continuously enhance auditing capabilities within regions
- Monitor regulatory trends and inspection outcomes to strengthen compliance and audit effectiveness
- Develops and maintains the global inspection readiness playbook, governance model, mock inspections, and readiness sprint methodology
- Design and deploy a structured, risk-based Global Mock inspection program
- Lead inspection readiness sprints prior to anticipated regulatory inspections with remediation prioritization
- Monitor global inspection outcomes and regulatory trends to strengthen defence capability
- Lead end-to-end execution of internal, supplier, distributor, and third-party audits for EMEAC
- Administer the global auditor qualification framework
- Provide guidance and system support to LATAM, US, JPAC regions
- Ensure traceability of audit activities, findings, and corrective actions with timely closure and consistent application of Good Practices
- Escalate critical regulatory compliance issues with global suppliers/vendors and define action plans
- Share audit trends and risk insights across regions to support inspection readiness
- Provide functional direction to regional audit leads regarding inspection readiness standards
Key requirements
- Minimum 10 years of audit management experience in a Pharma/Medical Devices environment
- Broad types of audits across cosmetics, medical devices, and pharmaceuticals
- Fluent English; additional languages a plus
- leadership
- cross-functional collaboration
- proactive problem solving
- audit management across regulated areas
- regulatory inspection readiness
- global auditor qualification framework
Global Quality Compliance Inspection Readiness & EMEAC Audits employer: Galderma
Galderma is an exceptional employer that prioritises employee growth and development within a dynamic and inclusive work culture. With a strong commitment to diversity and a focus on meaningful contributions to dermatology, employees are empowered to make a direct impact while enjoying the benefits of a hybrid working environment in vibrant locations like Zug, London, or Frankfurt. Join us to be part of a passionate team dedicated to advancing dermatology and enhancing lives across the EMEAC region.
StudySmarter Expert Advice🤫
We think this is how you could land Global Quality Compliance Inspection Readiness & EMEAC Audits
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Galderma. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Galderma.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Galderma. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Galderma is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Global Quality Compliance Inspection Readiness & EMEAC Audits
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Galderma!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Galderma that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Galderma!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Galderma, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Galderma
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Galderma that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Galderma’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
