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- Tasks: Lead quality assurance for a growing generics pharmaceutical manufacturer in Hertfordshire.
- Company: Join a dynamic team focused on improving pharmaceutical quality standards.
- Benefits: Enjoy a leadership role with opportunities for professional growth and development.
- Why this job: Make a real impact in the pharmaceutical industry while ensuring product safety and compliance.
- Qualifications: 5+ years in Quality Assurance, leadership experience, and a degree required.
- Other info: Ideal for seasoned professionals looking to advance their careers in a supportive environment.
The predicted salary is between 43200 - 72000 £ per year.
Exciting opportunity: Head of Quality for a growing generics pharmaceutical manufacturer.
If you are a seasoned Quality professional, based in or around Hertfordshire, with leadership experience in the pharmaceutical industry, this role might be for you!
Your Responsibilities:
- Responsible to oversee and continually review the quality management system to ensure that improvements are identified and that any deficiencies are addressed at their root cause and appropriate procedures are developed and fully implemented.
- Verify and ensure that the products are manufactured, packed and tested to the requirements of registered MA.
- Responsible to review the third-party audit reports for APIs and packaging materials. Responsible for the review of annual product quality reviews.
- Ensuring complaints and adverse incidents are accurately recorded and addressed in a thorough and timely manner in accordance with the company QMS.
- Responsible for hosting MHRA inspections, writing the response reports and to liaise with the Medicines Inspectorate to ensure that the Company conforms to the requirements of GMP and the Manufacturing and Product Licenses.
- Develop, manage and maintain the company's device family technical files and product specific design dossiers ensuring compliance with the relevant regulations.
- Remain up to date with impending changes and developments regarding regulatory and compliance requirements as well as evolving best practices in compliance control.
- To approve specifications, sampling instructions, test methods, and QC procedures, including amendments.
- To approve and monitor suppliers of raw materials and packaging components.
Your experince, skills and qualifications:
- A bachelors or associate degree.
- A minimum of 5 years experince in the Quality Assurance at a manufacturing site
- Previous experince in a leadership role.
- Extensive Pharmaceutical Industry experince with hands on experince in development/quality in a GxP environment.
If this sounds like the perfect opportunity for you or someone you know, please share your CV at !
Head of Quality Assurance employer: X4 Life Sciences
Contact Detail:
X4 Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Quality Assurance
✨Tip Number 1
Make sure to highlight your leadership experience in the pharmaceutical industry during networking events or informal meetups. Connecting with professionals in the field can give you insights into the company culture and expectations.
✨Tip Number 2
Stay updated on the latest regulatory changes and best practices in quality assurance. This knowledge will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 3
Consider reaching out to current or former employees of the company on LinkedIn. They can provide valuable information about the role and the company's approach to quality management.
✨Tip Number 4
Prepare specific examples from your past experiences that showcase your ability to address deficiencies in quality management systems. Being able to discuss these in detail will set you apart during the interview process.
We think you need these skills to ace Head of Quality Assurance
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in Quality Assurance, especially in the pharmaceutical industry. Emphasize your leadership roles and any specific achievements that demonstrate your ability to oversee quality management systems.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your passion for quality assurance and your understanding of the pharmaceutical sector. Mention specific experiences that relate to the responsibilities listed in the job description, such as handling MHRA inspections or managing third-party audits.
Highlight Relevant Qualifications: In your application, ensure you mention your educational background and any certifications related to quality assurance or regulatory compliance. This will help demonstrate your qualifications for the role.
Showcase Continuous Learning: Mention any recent training or courses you've completed that relate to quality management or regulatory changes in the pharmaceutical industry. This shows that you are proactive and committed to staying updated with industry best practices.
How to prepare for a job interview at X4 Life Sciences
✨Showcase Your Leadership Experience
Since the role requires leadership experience, be prepared to discuss specific examples of how you've successfully led teams in the past. Highlight your ability to motivate and guide others, especially in a quality assurance context.
✨Demonstrate Your Knowledge of Regulatory Compliance
Familiarize yourself with GMP and other relevant regulations. Be ready to discuss how you have ensured compliance in previous roles, and share any experiences you have had with MHRA inspections or similar audits.
✨Prepare for Technical Questions
Expect questions related to quality management systems and product quality reviews. Brush up on your technical knowledge regarding specifications, sampling instructions, and QC procedures to confidently answer these queries.
✨Discuss Continuous Improvement Initiatives
Be prepared to talk about how you've identified deficiencies in quality processes and implemented improvements. Share specific examples that demonstrate your proactive approach to enhancing quality management systems.
