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- Tasks: Lead and execute a quality strategy in a biopharmaceutical setting.
- Company: Mantell Associates specialise in Pharmaceutical and Life Sciences recruitment.
- Benefits: Join a senior leadership team with opportunities for professional growth.
- Why this job: Make a real impact on product quality and compliance in a dynamic industry.
- Qualifications: Bachelor’s degree in a scientific field and proven management experience in Quality.
- Other info: Collaborate with various departments to drive improvements and ensure compliance.
The predicted salary is between 43200 - 72000 £ per year.
Mantell Associates are partnered with a Biopharmaceutical organisation in their search for a Head of Quality to join their senior leadership team and build, lead and execute a quality strategy.
Head of Quality - Responsibilities:
- Responsible for all aspects of the Quality organisation, including Quality Assurance (QA), Quality Control (QC) and Quality Management System (QMS).
- Provide leadership and strategy to ensure that all products/services are aligned with quality standards, regulations (FDA and other notified regulatory bodies) and customer/regulatory requirements.
- Work closely with the senior Operations team to transform and create a culture of compliance excellence - reporting to the top management on performances/improvements.
- Ensure the site QMS is aligned with regulatory requirements and International Quality Standards.
- Work closely with the Manufacturing, Regulatory Affairs and other departments to make suggestions, set objectives and execute solutions for improvements in processes and compliance.
- Oversee team members and ensure performance levels meet corporate, Quality and business objectives.
Head of Quality - Requirements:
- Bachelor’s degree or higher in a scientific area.
- Proven experience in management and leading Quality in a technical manufacturing environment.
- Proven experience controlling Quality Management Systems (QMS) and with Good Manufacturing Practices (cGMPs).
- Excellent knowledge and previous collaboration with regulatory guidelines.
- Strong working knowledge of GxP and quality systems.
Risk Management & Quality Officer employer: Mantell Associates
Contact Detail:
Mantell Associates Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Risk Management & Quality Officer
✨Tip Number 1
Network with professionals in the biopharmaceutical industry, especially those who have experience in quality management. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in quality assurance and compliance.
✨Tip Number 2
Familiarise yourself with the specific regulatory guidelines relevant to the role, such as FDA regulations and international quality standards. This knowledge will not only boost your confidence but also demonstrate your commitment to quality excellence during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in managing Quality Management Systems (QMS) and how you’ve successfully implemented Good Manufacturing Practices (cGMPs). Be ready to provide examples of how you've led teams to achieve compliance and improve quality processes.
✨Tip Number 4
Research Mantell Associates and their client’s values and mission. Tailor your conversations to align with their goals, showcasing how your leadership style and quality strategy can contribute to their vision of compliance excellence.
We think you need these skills to ace Risk Management & Quality Officer
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Risk Management & Quality Officer position. Understand the key responsibilities and requirements, especially focusing on quality assurance, quality control, and quality management systems.
Tailor Your CV: Customise your CV to highlight relevant experience in quality management and compliance within a biopharmaceutical or technical manufacturing environment. Emphasise your leadership skills and any specific achievements related to quality standards and regulatory compliance.
Craft a Compelling Cover Letter: Write a cover letter that directly addresses how your background aligns with the responsibilities of the role. Mention your experience with QMS, cGMPs, and collaboration with regulatory bodies, showcasing your ability to lead and execute quality strategies.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. Ensure that your writing is clear and professional, as attention to detail is crucial in quality management roles.
How to prepare for a job interview at Mantell Associates
✨Understand the Quality Landscape
Familiarise yourself with the latest regulations and standards in the biopharmaceutical industry, especially those related to FDA guidelines and Good Manufacturing Practices (cGMPs). This knowledge will demonstrate your commitment to quality and compliance during the interview.
✨Showcase Leadership Experience
Prepare examples of how you've successfully led teams in a quality management context. Highlight specific instances where you transformed processes or improved compliance, as this aligns with the responsibilities of the Head of Quality role.
✨Collaborate Across Departments
Be ready to discuss your experience working with various departments such as Manufacturing and Regulatory Affairs. Emphasise your ability to foster collaboration and drive improvements across teams, which is crucial for the role.
✨Prepare for Scenario-Based Questions
Anticipate questions that may ask how you would handle specific quality-related challenges. Think through potential scenarios and your approach to problem-solving, ensuring you can articulate your thought process clearly.
