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- Tasks: Lead a small team in quality management for a global generics manufacturer.
- Company: Join RBW Consulting, a key player in the pharmaceutical industry.
- Benefits: Enjoy an attractive salary and comprehensive benefits package.
- Why this job: Make a real impact in quality assurance while working in a dynamic environment.
- Qualifications: Must have QP status and experience in non-sterile pharmaceutical manufacturing.
- Other info: This role is fully site-based with opportunities for coaching and mentoring.
The predicted salary is between 48000 - 72000 £ per year.
Partnering with a global generics manufacturer and distributor, we are supporting the search for a Head of Quality or Quality Director, depending on the level of experience. This role is fully site-based in the commercial offices, with some visibility of warehouses and distribution. Managing a small department, it requires a hands-on approach, with senior leadership involved in daily tasks. The technical scope includes operations, systems, auditing, and supplier management. With QP status, you will support existing QPs in the team. The position offers an attractive salary and benefits package.
Key experience:
- Eligibility to work as a QP in the UK
- Experience in non-sterile pharmaceutical manufacturing, ideally generics
- QA management and leadership experience
- A proactive, hands-on working style emphasizing coaching and mentoring
- Experience working with virtual teams overseas
Director of Quality employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director of Quality
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in quality management. Attend industry events or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest regulations and standards in non-sterile pharmaceutical manufacturing. Being knowledgeable about current compliance requirements will demonstrate your commitment to quality and safety.
✨Tip Number 3
Highlight your leadership skills by sharing examples of how you've successfully managed teams in previous roles. Emphasise your hands-on approach and ability to mentor others, as this is crucial for the Director of Quality position.
✨Tip Number 4
Research the company culture and values of the organisation you're applying to. Tailor your conversations during interviews to align with their mission, showcasing how your experience and philosophy fit into their vision.
We think you need these skills to ace Director of Quality
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Director of Quality position. Make sure you understand the key responsibilities and required experience, especially regarding QP status and QA management in non-sterile pharmaceutical manufacturing.
Tailor Your CV: Customise your CV to highlight relevant experience in quality assurance management, particularly in generics. Emphasise your leadership skills and any hands-on experience you have in coaching and mentoring teams.
Craft a Compelling Cover Letter: Write a cover letter that connects your background to the specific requirements of the role. Mention your eligibility to work as a QP in the UK and provide examples of your proactive approach in previous positions.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a quality management role.
How to prepare for a job interview at JR United Kingdom
✨Showcase Your Leadership Skills
As a Director of Quality, you'll be expected to lead a small department. Be prepared to discuss your previous leadership experiences, focusing on how you've successfully managed teams and mentored individuals in the past.
✨Demonstrate Technical Knowledge
Familiarise yourself with the technical aspects of quality assurance in non-sterile pharmaceutical manufacturing. Be ready to discuss specific systems, auditing processes, and supplier management strategies that you have implemented or improved in your previous roles.
✨Emphasise Your Hands-On Approach
This role requires a proactive, hands-on working style. Prepare examples of how you've been involved in daily tasks and operations, showcasing your ability to balance strategic oversight with practical involvement.
✨Prepare for Questions on Global Collaboration
Since the position involves working with virtual teams overseas, think about your experiences in collaborating across different cultures and time zones. Be ready to share how you’ve effectively communicated and coordinated with international teams.
