At a Glance
- Tasks: Lead the quality and regulatory affairs for Dräger's Safety Division in the UK.
- Company: Join Dräger, a global leader in medical and safety technology dedicated to saving lives.
- Benefits: Enjoy a full-time role with opportunities for professional growth and impactful work.
- Why this job: Make a difference in quality management while working with innovative teams and technologies.
- Qualifications: Experience in quality management and regulatory affairs is essential; leadership skills are a must.
- Other info: Located in Blyth, Northumberland, this role offers a chance to shape safety standards.
The predicted salary is between 48000 - 72000 £ per year.
At Dräger we protect, support and rescue lives day in and day out. We are interested in you if you have the desire to work for an organisation that does something more, something that is truly worth working for. As an international leader in medical and safety technology, we develop pioneering devices, software, services and solutions that people around the world trust. Wherever Dräger products are used, it’s about the most important thing: it’s about life. Employment Type: Full-Time Location: Blyth, Northumberland Postal Code: NE24 4BQ. About the role The Head of Quality & Regulatory Affairs manages the entire quality area of the Safety Division UK. The function ensures that demanding quality targets are realized and that the targeted economic goals (growth and profitability) are achieved. The area of responsibility includes Supplier Quality Assurance, Production Quality, and Quality & Regulatory Affairs including product quality and reliability engineering. The job holder will work very closely cross-functionally with colleagues in the Business Fields, Research & Development and Supply Chain of the Safety Division as well as Global Sales & Service and Quality in the Safety Division as well as Corporate Quality. General Responsibilities Overall management and leadership of the entire quality area of the Safety Division UK. Strategic, conceptional and operative management, leadership and development of Supplier Quality Assurance, Production Quality and Quality & Regulatory Affairs. Responsibility for the achievement of agreed targets and key performance indicators. Agreed targets and key performance indicators refer to quality key figures as well as the improvement in earnings (EBIT) of the related business. Operate and continuously improve the quality management system at all sites to sustainably support Dräger’s strategy and the company’s values. Ensure that Dräger Safety’s UK Ltd.’s quality management system is compliant with the various relevant regulatory and legal requirements and standards. Provide leadership to the quality functions ensuring there is a clear and common objective, guidelines, and priorities. Develop the staff working in quality functions so they have the skills and competencies required to perform their roles. Monitor performance of quality staff and improve where necessary, if necessary, taking disciplinary action. Representation of Dräger Safety UK Ltd. in internal and external audits. Quality / Environmental Management System Implement corporate standards into the localised Integrated Management System within the specified effective date, improve and monitor effectiveness of the IMS. Ensure compliance with relevant directives, standards, technical and regulatory requirements and assure the achievement of quality and environmental targets. Implement and maintain an internal audit program. Ensure that external certification/approvals are maintained, addressing any identified nonconformities within the timescales specified. Generate Quality and Environmental targets and initiatives to support the business needs based on corporate, regulatory, and local requirements. Report performance against these targets and initiate corrective action when required. Communicate within the leadership team and throughout the business to ensure that the Quality and Environmental ethos is shared and maintained. Advises Q&RA and other functions regarding the development and implementation of new government/regulatory developments and regulatory strategy. Develop, implement, and review current policies and practices issued by regulatory agencies. Participate in industry groups to ensure Company is kept current on all pending regulatory changes and that the Company position is made known and/or represented. Product Quality, Supplier Quality Assurance, Production Quality and Safety Define demanding quality targets, analyse, and measure performance, improve where required (e.g., by using CAPA), control the effectiveness. Assure high product quality in Sourcing and Production and by early involvement in the new product development process by the deployment of Reliability Engineers and implementation of the new product development process supported by best practice methods and tools. Ensure that Customer claims are handled in an effective and efficient manner to the timely satisfaction of the Customer. Promote awareness of customer requirements, monitor quality performance, and communicate customer quality issues and resolution thereof. Conduct the market surveillance, therefore closely interact with corporate partners, e.g., subsidiaries, and generate product improvement programs in close cooperation with involved functions as e.g., R&D, Production, Purchasing and Product Management. Generate product improvement programs in close cooperation with relevant functions. Assure device vigilance and complaint handling responsibilities. Assure fulfilment of device reporting responsibilities. Maintaining and deploying an analytical approach to problem solving utilising the recognised techniques of Lean Six Sigma, 8D, etc. Leadership in continuous improvement initiatives to meet business needs. Assure that product quality requirements are fully implemented at every location that manufactures/modifies (LVA) CABE products. #J-18808-Ljbffr
Head of Quality & Regulatory Affairs employer: Laraveldaily
Contact Detail:
Laraveldaily Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Quality & Regulatory Affairs
✨Tip Number 1
Familiarize yourself with the latest regulations and standards in quality and regulatory affairs specific to the medical technology industry. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the quality and regulatory affairs sector, especially those who work in medical technology. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the field.
✨Tip Number 3
Prepare to discuss your experience with quality management systems and how you've successfully implemented improvements in previous roles. Be ready to share specific examples that highlight your leadership skills and ability to meet demanding quality targets.
✨Tip Number 4
Research Dräger's products and their impact on safety and medical technology. Understanding the company's mission and values will allow you to align your responses during interviews and show that you're genuinely interested in contributing to their goals.
We think you need these skills to ace Head of Quality & Regulatory Affairs
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Head of Quality & Regulatory Affairs position. Tailor your application to highlight relevant experiences that align with the job description.
Highlight Leadership Experience: Since this role involves overall management and leadership, emphasize your previous leadership roles and how you've successfully managed teams in quality assurance or regulatory affairs.
Showcase Relevant Achievements: Include specific examples of how you've achieved demanding quality targets or improved quality management systems in past positions. Use metrics to quantify your success where possible.
Tailor Your CV and Cover Letter: Customize your CV and cover letter to reflect the key responsibilities mentioned in the job description. Use similar language and terminology to demonstrate your understanding of the industry and the role.
How to prepare for a job interview at Laraveldaily
✨Understand Dräger's Mission
Before the interview, familiarize yourself with Dräger's commitment to protecting and supporting lives. Be prepared to discuss how your values align with their mission and how you can contribute to their goals in quality and regulatory affairs.
✨Showcase Your Leadership Experience
As the Head of Quality & Regulatory Affairs, strong leadership skills are essential. Prepare examples from your past experiences where you successfully managed teams, implemented quality systems, or led cross-functional projects that resulted in measurable improvements.
✨Demonstrate Knowledge of Regulatory Standards
Be ready to discuss relevant regulatory requirements and standards that impact the medical and safety technology industry. Highlight your experience in ensuring compliance and how you've navigated complex regulatory landscapes in previous roles.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities and decision-making skills. Think of specific situations where you had to address quality issues, manage audits, or implement corrective actions, and be ready to explain your thought process and outcomes.