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- Tasks: Ensure quality standards for medicinal products and perform batch release activities.
- Company: Join TFS HealthScience, a global leader in clinical research.
- Benefits: Competitive pay, professional growth, and a collaborative work environment.
- Why this job: Make a real impact on patient health while working with top pharmaceutical companies.
- Qualifications: Must be a legally qualified QP in the UK with pharma experience.
- Other info: Part-time role with flexible working arrangements and a focus on innovation.
The predicted salary is between 36000 - 60000 £ per year.
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.
The Qualified Person (QP) will be responsible for ensuring that medicinal products meet all required quality standards prior to release. This includes GMP oversight, batch certification, and compliance with UK and EU regulatory requirements.
As part of our SRS/FSP team, you will be dedicated to one sponsor in the UK, a well-established pharmaceutical company with a strong presence in health and nutrition. This position is part-time, approximately 0.2 FTE.
Key Responsibilities- Perform QP certification and batch release activities in accordance with UK and EU GMP.
- Ensure compliance with GMP, internal procedures, and current regulatory standards.
- Review and approve manufacturing documentation, deviations, CAPA, and change controls.
- Provide expert GMP and quality guidance to sponsor teams and stakeholders.
- Support internal and external audits, inspections, and regulatory interactions.
- Maintain oversight of quality systems related to product release.
- Legally eligible to act as a Qualified Person (QP) in the UK under the Human Medicines Regulations.
- Proven experience in pharmaceutical quality assurance and QP batch release.
- Strong knowledge of UK and EU GMP and associated regulatory requirements.
- Experience collaborating with manufacturing sites, CMOs, and cross-functional teams.
- Excellent communication, documentation, and decision-making skills.
- Ability to work independently with limited on-site requirements.
We provide a competitive compensation package and the opportunity for professional growth in a rewarding environment. You’ll join a team that values collaboration, innovation, and making a difference in the lives of patients.
Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working toward a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.
Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decision-making at all levels. These values foster a culture of collaboration, innovation, and excellence. Together, we make a difference.
Qualified Person - UK in London employer: TFS HealthScience
Contact Detail:
TFS HealthScience Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person - UK in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those who work as Qualified Persons. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and regulatory requirements. Be ready to discuss real-life scenarios where you've ensured compliance or handled quality assurance challenges. Show us your expertise and confidence!
✨Tip Number 3
Don’t just apply anywhere—focus on companies that align with your values and career goals. Check out our website for openings at TFS HealthScience and tailor your approach to highlight how you can contribute to our mission of improving patient lives.
✨Tip Number 4
Follow up after interviews! A simple thank-you email can go a long way in keeping you top of mind. Reiterate your enthusiasm for the role and remind us why you’re the perfect fit for the Qualified Person position.
We think you need these skills to ace Qualified Person - UK in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in pharmaceutical quality assurance and QP batch release. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Qualified Person role. Share your passion for quality assurance and how you can contribute to our mission at TFS HealthScience.
Showcase Your Regulatory Knowledge: Since this role involves compliance with UK and EU GMP, make sure to highlight your knowledge of these regulations in your application. We’re looking for someone who can navigate the complexities of regulatory requirements with ease!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at TFS HealthScience!
How to prepare for a job interview at TFS HealthScience
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practice (GMP) and the specific regulatory requirements in the UK and EU. Be prepared to discuss how you've applied these standards in your previous roles, as this will show your expertise and readiness for the Qualified Person position.
✨Showcase Your Experience
Highlight your proven experience in pharmaceutical quality assurance and batch release during the interview. Use specific examples from your past work to demonstrate how you've successfully navigated challenges and ensured compliance with quality standards.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your decision-making skills and ability to handle deviations or CAPAs. Think through potential situations you might face in the role and how you would respond, showcasing your problem-solving abilities and adherence to quality protocols.
✨Communicate Clearly and Confidently
Since excellent communication is key in this role, practice articulating your thoughts clearly and confidently. Be ready to explain complex concepts in a straightforward manner, as you'll need to provide guidance to sponsor teams and stakeholders effectively.
