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- Tasks: Join us as a Qualified Person, ensuring product quality and compliance in a dynamic pharmaceutical environment.
- Company: Smart4Sciences is a leading pharmaceutical company focused on innovation and quality in the North East.
- Benefits: Enjoy competitive pay, professional growth opportunities, and a collaborative work culture.
- Why this job: Make a real impact in healthcare by ensuring the safety and efficacy of sterile products.
- Qualifications: Must be a Certified Qualified Person with experience in GMP regulations and sterile products.
- Other info: This is an urgent role with immediate interviews—apply now to seize this opportunity!
The predicted salary is between 43200 - 72000 £ per year.
Smart4Sciences – Qualified Person Smart4Sciecnes are currently recruiting a Qualified Person to join a Pharmaceutical Company in the North East. 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 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…
Qualified Person QP employer: Science Solutions Recruitment
Contact Detail:
Science Solutions Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person QP
✨Tip Number 1
Make sure to highlight your experience with GMP regulations and sterile pharmaceutical products during the interview. Be prepared to discuss specific examples of how you've ensured compliance in previous roles.
✨Tip Number 2
Familiarize yourself with the Human Medicines Regulations and be ready to explain how you would apply these in your role as a QP. This shows your commitment to understanding the regulatory landscape.
✨Tip Number 3
Demonstrate your leadership skills by discussing any relevant experiences where you led a team or managed projects. This will help you stand out, especially since leadership experience is preferred for this position.
✨Tip Number 4
Prepare for questions about customer visits and audits. Think of instances where you successfully supported these processes, as this is a key responsibility of the role.
We think you need these skills to ace Qualified Person QP
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Qualified Person as outlined in the job description. Familiarize yourself with GMP regulations and the specific requirements for batch certification and release.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience with releasing pharmaceutical products and any leadership roles you've held. Be specific about your familiarity with sterile pharmaceutical products and how it relates to the position.
Tailor Your Application: Customize your application materials to reflect the key requirements mentioned in the job description. Use keywords from the listing to demonstrate that you meet the qualifications and are a good fit for the company.
Proofread Your Documents: Before submitting your application, 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 pharmaceutical industry.
How to prepare for a job interview at Science Solutions Recruitment
✨Understand GMP Regulations
Make sure you have a solid grasp of Good Manufacturing Practice (GMP) regulations, especially Annex 16. Be prepared to discuss how you've applied these regulations in your previous roles.
✨Showcase Your Leadership Skills
Since leadership experience is preferred, think of examples where you've successfully led a team or project. Highlight your ability to manage and motivate others in a high-stakes environment.
✨Prepare for Technical Questions
Expect technical questions related to batch certification and release processes. Brush up on your knowledge of sterile pharmaceutical products and be ready to explain your experience with them.
✨Demonstrate Your QA Support Experience
Be ready to discuss your experience providing QA support to manufacturing and packaging. Share specific examples of how you've ensured compliance with regulatory requirements during audits or customer visits.
