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For Companies At a Glance
- Tasks: Lead the Quality Assurance team and ensure compliance with pharmaceutical regulations.
- Company: Join a dynamic pharmaceutical company based in Central London, committed to product quality and safety.
- Benefits: Enjoy hybrid work options, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in a fast-paced environment while fostering a culture of excellence.
- Qualifications: Strong knowledge of GMP, GDP, and GPvP; degree in Life Sciences required.
- Other info: Ideal for results-driven leaders looking to advance their careers in quality assurance.
The predicted salary is between 43200 - 72000 £ per year.
We are looking for a Quality Assurance Lead to oversee compliance, risk management, and continuous improvement within our pharmaceutical operations. This role ensures that all GMP, GDP, and GPvP regulations are met while maintaining the highest standards of product quality and safety.
Key Responsibilities
- Leadership & Compliance
- Lead and develop the Quality Assurance team, fostering a culture of accountability and excellence.
- Maintain compliance as a Manufacturing Authorization Holder (MAH), ensuring adherence to all GxP standards.
- Oversee regulatory inspections, audits, and quality risk assessments, ensuring timely implementation of corrective and preventive actions (CAPAs).
- Act as the primary liaison with regulatory agencies and external stakeholders on quality matters.
- Quality Management & Continuous Improvement
- Manage and enhance the Quality Management System (QMS), including SOPs, documentation, and QMS improvements.
- Implement risk assessments and mitigation strategies throughout the product lifecycle.
- Drive compliance initiatives through internal training, education, and process improvement programs.
- Monitor and report on quality metrics (KPIs), including deviation rates, CAPAs, and customer complaints.
- Operational Oversight
- Ensure adherence to standard operating procedures in line with GMP, GDP, and GPvP practices.
- Manage product quality complaints, supplier qualifications, and technical agreements with third-party service providers.
- Support cross-functional teams, including supply chain, pharmacovigilance, regulatory affairs, and manufacturing, to align quality objectives.
- Ensure compliance with change controls, deviations, non-conformances, and internal audit observations.
About You
- Strong knowledge of GDP, GMP, and GPvP in the pharmaceutical industry.
- Experience leading quality teams with a proven track record in compliance and regulatory affairs.
- Eligible or experienced Responsible Person (RP) and Responsible Person for Import (RPi).
- Familiarity with QMS, risk management, CAPAs, and supplier oversight.
- Strong analytical, communication, and leadership skills with the ability to influence at all levels.
- Degree in Life Sciences or equivalent.
If you are a results-driven quality leader ready to take on a high-impact role in a fast-paced, compliance-driven environment, we would love to hear from you. Apply now or reach out for a confidential discussion.
Head of Quality - RPi employer: SKC Recruitment
Contact Detail:
SKC Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Quality - RPi
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in quality assurance roles. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in GMP, GDP, and GPvP compliance.
✨Tip Number 2
Familiarise yourself with the specific regulations and standards that govern quality assurance in pharmaceuticals. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality standards.
✨Tip Number 3
Prepare to discuss your leadership style and how you've successfully managed quality teams in the past. Be ready to share examples of how you've implemented CAPAs and improved QMS processes, as these are crucial for the role.
✨Tip Number 4
Research StudySmarter's values and culture to align your approach during the interview. Show how your personal values resonate with ours, particularly in fostering a culture of accountability and excellence within quality assurance.
We think you need these skills to ace Head of Quality - RPi
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in quality assurance, compliance, and leadership within the pharmaceutical industry. Use specific examples that demonstrate your knowledge of GMP, GDP, and GPvP regulations.
Craft a Compelling Cover Letter: In your cover letter, express your passion for quality assurance and how your background aligns with the responsibilities of the Head of Quality role. Mention your experience with regulatory inspections and CAPAs to showcase your suitability.
Highlight Relevant Skills: Emphasise your analytical, communication, and leadership skills in both your CV and cover letter. Provide examples of how you've influenced teams and driven compliance initiatives in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the quality assurance field.
How to prepare for a job interview at SKC Recruitment
✨Showcase Your Leadership Skills
As a Head of Quality, you'll need to demonstrate your ability to lead and develop teams. Prepare examples of how you've fostered a culture of accountability and excellence in previous roles, highlighting specific achievements.
✨Understand Regulatory Standards
Make sure you have a solid grasp of GMP, GDP, and GPvP regulations. Be ready to discuss how you've ensured compliance in past positions and how you would approach regulatory inspections and audits.
✨Emphasise Continuous Improvement
Discuss your experience with Quality Management Systems (QMS) and how you've implemented improvements. Be prepared to share specific strategies you've used for risk assessments and CAPA management.
✨Prepare for Cross-Functional Collaboration
This role requires working closely with various departments. Think of examples where you've successfully collaborated with supply chain, pharmacovigilance, or regulatory affairs teams to achieve quality objectives.
