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- Tasks: Join our team as a Quality Assurance Manager, ensuring product quality and compliance.
- Company: We specialise in advanced sterile products, driving growth in the manufacturing sector.
- Benefits: Enjoy flexible working hours and receive specialised training in a sterile environment.
- Why this job: Be part of a growing team with opportunities to engage in exciting projects post-training.
- Qualifications: Must be a qualified person (QP) with knowledge of GMP and sterile manufacturing.
- Other info: No management duties; focus on quality assurance and product release.
The predicted salary is between 36000 - 60000 £ per year.
We are now looking to speak with QPs across the UK for at least three brand new positions that are being hired due to an increase in manufacturing operations.
Having successfully partnered with this business to hire a number of critical positions due to expansion and increased product demand, these most recent requirements are the start of a new phase of growth in the Quality team.
The business specialises within advanced sterile products and will require QPs that are flexible to be based on site for releasing activities and who can be flexible on starting hours. Given the nature of the product, the company offers a fantastic opportunity for specific product training in a sterile manufacturing environment.
There will be no management responsibilities associated with the role but, as well as the releasing duties, QPs will have the opportunity to get involved in key projects for the business once training is completed.
Quality Assurance Manager & Qualified Person employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Manager & Qualified Person
✨Tip Number 1
Familiarise yourself with the specific regulations and guidelines related to sterile manufacturing and GMP. Understanding the MHRA requirements will not only boost your confidence but also demonstrate your commitment to quality assurance in the interview.
✨Tip Number 2
Network with professionals in the pharmaceutical and sterile manufacturing sectors. Attend industry events or join relevant online forums to connect with others who can provide insights into the role and potentially refer you to opportunities at StudySmarter.
✨Tip Number 3
Prepare to discuss your flexibility regarding working hours and on-site responsibilities. Highlighting your willingness to adapt to the needs of the business will show that you are a team player and ready to contribute to their growth.
✨Tip Number 4
Research the company’s recent projects and initiatives in sterile product development. Being knowledgeable about their work will allow you to ask informed questions during the interview, showcasing your genuine interest in the position and the company.
We think you need these skills to ace Quality Assurance Manager & Qualified Person
Some tips for your application 🫡
Understand the Role: Familiarise yourself with the responsibilities of a Qualified Person in a sterile manufacturing environment. Highlight your understanding of GMP and the importance of quality assurance in your application.
Tailor Your CV: Make sure your CV reflects relevant experience in quality assurance and any specific training related to sterile products. Emphasise your flexibility and willingness to adapt to the company's needs.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your qualifications and how they align with the job requirements, particularly your experience with audits and product release.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, as attention to detail is crucial in quality assurance roles.
How to prepare for a job interview at RBW Consulting
✨Understand the Role of a Qualified Person
Make sure you have a solid grasp of what a Qualified Person does, especially in a sterile manufacturing environment. Familiarise yourself with GMP regulations and the specific responsibilities related to product release and quality assurance.
✨Show Flexibility and Adaptability
Since the role requires flexibility in working hours and on-site presence, be prepared to discuss your availability and willingness to adapt to the company's needs. Highlight any previous experiences where you successfully adapted to changing circumstances.
✨Prepare for Technical Questions
Expect to face technical questions related to quality assurance and sterile manufacturing processes. Brush up on your knowledge of terminally sterilised products and aseptic techniques, as well as any relevant audits or compliance standards.
✨Express Interest in Continuous Learning
The company offers specific product training, so convey your enthusiasm for ongoing professional development. Share examples of how you've pursued learning opportunities in the past and how you plan to continue growing in this role.
