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- Tasks: Join our team as a Qualified Person, reviewing and certifying medical product batches.
- Company: Smart4Sciences is a dynamic clinical trials company based in South Wales.
- Benefits: Gain valuable experience with progression opportunities to Quality Director roles.
- Why this job: Be part of a strong release team and contribute to impactful healthcare solutions.
- Qualifications: Must be a Certified Qualified Person; leadership experience preferred.
- Other info: This is an urgent requirement with immediate interviews available.
The predicted salary is between 36000 - 60000 £ per year.
Smart4Sciences – QP Smart4Sciences are currently recruiting a Qualified Person to join a clinical trials company based in South Wales. This would a brilliant opportunity for a recently certified QP to join a strong release team while gaining experience on a license for the first time with progression aspirations to Quality Director level positions 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 performing batch review and certification of both sterile and non-sterile investigational medical products Issue and review approved documentation to support operational teams Provide support to Operations Staff and other QPs regarding all quality matters Support site QA teams when hosting audits Contribute to daily, monthly and quarterly operations and quality update meetings Conduct audits of suppliers across UK, EU and further global marketsKey Requirements You must be a Certified Qualified Person Leadership/line management experience is preferred Experience with Sterile Pharmaceutical products is preferredThis Qualified Person vacancy is an urgent requirement with interviews happening now – if you would be interested please apply today
Qualified Person employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person
✨Tip Number 1
Make sure to familiarize yourself with the latest GMP guidelines and Human Medicines Regulations. This knowledge will not only help you in your role but also impress the interviewers with your commitment to compliance.
✨Tip Number 2
Network with other Qualified Persons and professionals in the clinical trials field. Attend industry events or join relevant online forums to connect with others who can provide insights and potentially refer you to opportunities.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled batch reviews and certifications in the past. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills.
✨Tip Number 4
Show your enthusiasm for growth within the company. Express your aspirations to progress to Quality Director level positions during the interview, as this aligns with the company's goals and shows your long-term commitment.
We think you need these skills to ace Qualified Person
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. Highlight your relevant experience with batch review, certification, and GMP compliance in your application.
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 roles you've held.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for quality assurance and your aspirations to progress to a Quality Director level. Mention how your skills align with the company's needs and your eagerness to contribute to their team.
Highlight Relevant Certifications: Clearly list your certifications and any additional training related to quality assurance and regulatory compliance. This will help demonstrate your qualifications and commitment to the role.
How to prepare for a job interview at Smart4Sciences
✨Understand GMP and Regulations
Make sure you have a solid understanding of Good Manufacturing Practices (GMP) and the Human Medicines Regulations. Be prepared to discuss how these regulations impact your role as a Qualified Person and provide examples from your experience.
✨Showcase Your Leadership Skills
Since leadership experience is preferred, think of specific instances where you've demonstrated leadership or line management skills. Be ready to share how you can contribute to the team and support operations staff effectively.
✨Prepare for Technical Questions
Expect technical questions related to batch review and certification processes for both sterile and non-sterile products. Brush up on your knowledge of the specific requirements and challenges associated with these processes.
✨Demonstrate Your Audit Experience
If you have experience conducting audits, be prepared to discuss this in detail. Highlight any audits you've performed, particularly those involving suppliers across different markets, and how you ensured compliance with quality standards.
