Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: As a QP, you'll review batch records and certify sterile products.
- Company: Join Smart4Sciences, a leading Aseptic Pharmaceutical company in the West Midlands.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and development.
- Why this job: Make a real impact in the pharmaceutical industry while ensuring product safety and compliance.
- Qualifications: Must be a Certified Qualified Person with experience in GMP regulations.
- Other info: This is an urgent role with immediate interviews available—apply now!
The predicted salary is between 36000 - 60000 £ per year.
Smart4Sciences – QP Smart4Sciences are currently recruiting a Qualified Person to join an Aseptic Pharmaceutical company in the West Midlands. As a QP you will be responsible for reviewing and evaluating batch records and performing batch certification and release of sterile products in accordance with GMP and the Human Medicines Regulations. Key Responsibilities Act as QP for all products manufactured and packaged at the site; in accordance with marketing authorisations and manufacturing licences Provide QA Support to manufacturing, packaging and supply chain Assure product, process and facilities comply with national and international regulatory requirements Provide support for customer visits and audits while also conducting external audits of suppliers, vendors and service providers Key Requirements You must be a Certified Qualified Person Experience releasing pharmaceutical products in accordance with Annex 16 GMP regulations and Leadership/line management experience is preferred Experience with Sterile Pharmaceutical products is preferred This Qualified Person vacancy is an urgent requirement with interviews happening now – if you would be interested please apply today
QP employer: Science Solutions Recruitment
Contact Detail:
Science Solutions Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QP
✨Tip Number 1
Make sure to familiarize yourself with the latest GMP regulations and Annex 16 requirements. This knowledge will not only help you during the interview but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Highlight any experience you have with sterile pharmaceutical products in your discussions. Be prepared to share specific examples of how you've ensured compliance and quality in previous roles.
✨Tip Number 3
Since this role involves customer visits and audits, practice articulating your approach to quality assurance and how you handle external audits. This will show your confidence and readiness for the responsibilities of a QP.
✨Tip Number 4
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. They can provide valuable insights and may even refer you to opportunities within their organizations.
We think you need these skills to ace QP
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Qualified Person (QP) as outlined in the job description. Highlight your relevant experience in reviewing batch records and ensuring compliance with GMP and Human Medicines Regulations.
Tailor Your CV: Customize your CV to emphasize your qualifications as a Certified Qualified Person. Include specific examples of your experience with sterile pharmaceutical products and any leadership or line management roles you've held.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the pharmaceutical industry. Mention your experience with Annex 16 GMP regulations and how you can contribute to the company's success.
Highlight Regulatory Knowledge: In your application, make sure to highlight your knowledge of national and international regulatory requirements. This is crucial for the QP role and will demonstrate your suitability for the position.
How to prepare for a job interview at Science Solutions Recruitment
✨Know Your GMP Regulations
Make sure you are well-versed in GMP regulations, especially Annex 16. Be prepared to discuss how you've applied these regulations in your previous roles.
✨Demonstrate Your QA Support Experience
Highlight your experience in providing QA support to manufacturing and packaging processes. Share specific examples of how you've ensured compliance with regulatory requirements.
✨Prepare for Audits
Since the role involves conducting external audits, be ready to talk about your audit experiences. Discuss how you handle customer visits and what steps you take to ensure a smooth audit process.
✨Showcase Leadership Skills
If you have leadership or line management experience, make sure to emphasize it. Discuss how you've led teams or projects in the past and how that experience can benefit the company.
