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For Companies At a Glance
- Tasks: Oversee batch release and ensure quality standards in a dynamic pharmaceutical environment.
- Company: Join a rapidly expanding pharmaceutical company with a strong reputation for quality.
- Benefits: Competitive salary, supportive team culture, and opportunities for professional growth.
- Why this job: Be part of a crucial role that impacts production efficiency and quality assurance.
- Qualifications: Must be a UK Qualified Person with GMP experience in non-sterile products.
- Other info: Work five days a week on-site in Liverpool, contributing to a robust quality foundation.
The predicted salary is between 68000 - 95000 £ per year.
£80,000 - £95,000 per year
Liverpool, UK
An ideal batch release opportunity has become available at a pharmaceutical manufacturing client of ours. This company has been on an expansion trajectory and is looking to grow further over the next few years. As part of their planned expansion, they first want to introduce a solid and robust Quality foundation to build off of.
With the addition of this QP, the quality team will be in an increasingly positive position to release a higher level of batches and keep up with the exceptional efficiency of production, whilst also ensuring that nothing is missed within QA when it comes to release.
Things a QP might want to know:
- This company has a positive relationship with the MHRA and is not in IAG or Remediation processes. They have always kept on the right side of the rules and they have a robust and efficient QMS.
- The role oversees two main sites, a manufacturing site and an importation site.
- Dosage form: Oral Liquids.
- The QA team is around 5 people as stands, with 1-2 looking to join this year.
The Role
This position is primarily a batch release focussed role, with some light QMS and line management / mentorship opportunities folded into the responsibilities along the way. This position is key to the company’s release activities as currently QPs are releasing an immense quantity of batches and as the business grows this is set to increase.
The Requirements
- Must be a UK Qualified Person already listed on a UK licence.
- Must have experience of a GMP site as a QP.
- Must be experienced in Non-Sterile Products as a QP.
- Ideally have some exposure to Parallel Importation / Virtual Manufacturing Environments.
- Available to work 5 days on site in the Liverpool, UK area.
Click APPLY NOW, or call +44 (0) (phone number removed).
Full Time | Permanent Role | Certified QP Only | Based in Liverpool five days per week | APPLY NOW
Qualified Person employer: ARx Recruitment Services
Contact Detail:
ARx Recruitment Services Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. Attend industry events or join relevant online forums to connect with potential colleagues and learn more about the company culture.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines set by the MHRA, as well as the company's Quality Management System (QMS). This knowledge will not only help you during interviews but also demonstrate your commitment to maintaining high standards in batch release.
✨Tip Number 3
Prepare to discuss your experience with non-sterile products and any exposure to parallel importation or virtual manufacturing environments. Highlighting these experiences can set you apart from other candidates and show that you understand the complexities of the role.
✨Tip Number 4
Be ready to showcase your leadership and mentorship skills, as the role involves some line management responsibilities. Think of examples from your past where you've successfully guided a team or improved processes, as this will be valuable in demonstrating your fit for the position.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Qualified Person. Familiarise yourself with batch release processes, GMP standards, and the specific needs of the pharmaceutical industry.
Tailor Your CV: Highlight your relevant experience as a Qualified Person, especially in GMP environments and with non-sterile products. Make sure to include any specific achievements or contributions you've made in previous roles that align with the job description.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are the ideal candidate for this position. Mention your qualifications, experience, and how you can contribute to the company's growth and quality assurance efforts.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in the role of a Qualified Person.
How to prepare for a job interview at ARx Recruitment Services
✨Know Your Regulations
As a Qualified Person, it's crucial to have a solid understanding of the regulations governing pharmaceutical manufacturing. Brush up on your knowledge of MHRA guidelines and ensure you can discuss how you've adhered to these in your previous roles.
✨Demonstrate Your Experience
Be prepared to share specific examples from your experience in GMP environments. Highlight your role in batch release processes and any challenges you've faced, along with how you overcame them.
✨Showcase Your Leadership Skills
Since this role involves some mentorship opportunities, be ready to discuss your leadership style. Share instances where you've successfully guided team members or improved team performance in quality assurance.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality management system and their expansion plans. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
