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- Tasks: Join our Quality team as a Qualified Person, focusing on releasing activities and key projects.
- Company: We specialise in advanced sterile products and are expanding due to increased demand.
- Benefits: Receive specific product training and enjoy flexible working hours with no management responsibilities.
- Why this job: Be part of a growing team in a dynamic environment that values your contributions.
- Qualifications: Eligible QP status in the UK; experience in sterile manufacturing is a plus but not essential.
- Other info: Contact Mark Bux-Ryan for more details about this exciting opportunity.
The predicted salary is between 36000 - 60000 £ per year.
Qualified Person (QP)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. Experience:Eligible QP status within the UKExperience in sterile manufacturing preferred but not essentialEligibility as an RP is a nice to have but is not essentialStrong stakeholder skills with the ability to work in a small and dynamic teamWillingness and flexibility to be on site as required for releasing dutiesGiven the nature of the operations, if you would like to discuss this further, please contact Mark Bux-Ryan for further information.QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release, production
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP)
✨Tip Number 1
Network with professionals in the pharmaceutical and sterile manufacturing sectors. Attend industry events or join relevant online forums to connect with QPs and learn about their experiences, which can give you insights into what the hiring company values.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to sterile manufacturing and quality assurance. Being knowledgeable about GMP and MHRA standards will demonstrate your commitment to the role and help you stand out during discussions.
✨Tip Number 3
Prepare to discuss your flexibility and willingness to adapt to the dynamic nature of the role. Highlight any previous experiences where you successfully managed changing priorities or worked in fast-paced environments.
✨Tip Number 4
Research the company’s recent projects and initiatives in sterile product manufacturing. Showing that you understand their business and are genuinely interested in contributing to their growth can make a positive impression during your conversations.
We think you need these skills to ace Qualified Person (QP)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Qualified Person (QP) in a sterile manufacturing environment. Familiarise yourself with the specific requirements mentioned in the job description.
Highlight Relevant Experience: In your CV and cover letter, emphasise any relevant experience you have in sterile manufacturing or related fields. Even if you don't have direct experience, showcase transferable skills that demonstrate your capability to adapt to this role.
Tailor Your Application: Customise your application materials to reflect the specific needs of the company. Mention your flexibility regarding on-site duties and your willingness to engage in key projects after training.
Proofread Your Documents: Ensure that your CV and cover letter are free from errors. A well-presented application reflects your attention to detail, which is crucial for a role in quality assurance.
How to prepare for a job interview at LinkedIn
✨Understand the Role of a QP
Make sure you have a solid grasp of what a Qualified Person does, especially in a sterile manufacturing environment. Familiarise yourself with the responsibilities related to product release and quality assurance, as well as any relevant regulations.
✨Showcase Your Flexibility
Since the role requires flexibility regarding on-site presence and working hours, be prepared to discuss your availability and willingness to adapt. Highlight any previous experiences where you successfully managed changing schedules or environments.
✨Emphasise Stakeholder Skills
The ability to work effectively within a small team is crucial. Prepare examples that demonstrate your strong stakeholder management skills and how you've collaborated with others to achieve common goals in past roles.
✨Prepare for Technical Questions
Expect questions related to GMP and sterile manufacturing processes. Brush up on your technical knowledge and be ready to discuss any relevant experience, even if it's not directly from a QP role. This will show your commitment to the field.
