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- Tasks: Act as a Qualified Person, ensuring compliance and releasing high-quality pharmaceutical products.
- Company: Join Smart4 Sciences, a leading pharmaceutical organisation focused on quality and innovation.
- Benefits: Enjoy remote work flexibility with only one day on-site per month.
- Why this job: Be part of a supportive culture in a growing company with a strong reputation.
- Qualifications: Must be eligible as a Qualified Person in the UK with GMP knowledge.
- Other info: Perfect for those seeking autonomy and a collaborative work environment.
The predicted salary is between 36000 - 60000 £ per year.
Smart4 Sciences – Qualified Person (QP) – Remote Working (Permanent) Are you an experienced QP looking for a fully remote opportunity? Smart4 Sciences are partnering with a leading pharmaceutical organisation to recruit a Qualified Person (QP) for a permanent remote-based role. Whether you have just passed your Viva or have prior experience on a licence; this is an excellent opportunity for a QP who enjoys autonomy and flexibility while contributing to the release of high-quality pharmaceutical products under a Manufacturer\’s/Importer\’s Authorisation (MIA) licence. Key Responsibilities: Act as a Named Qualified Person under the MIA licence, in compliance with EU GMP and UK regulatory standards. Perform final certification and batch release of medicinal products (both sterile and non-sterile, depending on experience). Review batch documentation, quality records, and deviation/CAPA reports as part of batch release process. Collaborate with Quality Assurance, Production, and Regulatory teams to ensure GMP compliance across the supply chain. Support inspections from the MHRA and other regulatory bodies as required. Provide expert QP input into quality system improvements and GMP compliance strategies. Ideal Candidate: Eligible to act as a Qualified Person in the UK under Directive 2001/83/EC. Prior experience releasing products under an MIA licence is preferred Strong understanding of GMP and UK pharmaceutical regulatory frameworks. Excellent attention to detail and ability to work independently in a remote setting. Strong communication skills and a collaborative approach to cross-functional working. Why Apply? Remote working – achieve true work/life balance (1 day per month on site in England) Be part of a growing, quality-driven pharmaceutical business with a strong reputation. Join a forward-thinking organisation with a collaborative and supportive culture.If you are a QP eager to work remotely please apply now or contact Gareth Gooley on today for a confidential discussion
Qualified Person - Pharmaceuticals - Remote Working employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person - Pharmaceuticals - Remote Working
✨Tip Number 1
Familiarise yourself with the specific regulatory frameworks and guidelines that govern Qualified Persons in the UK, particularly Directive 2001/83/EC. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during any discussions.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. Engaging in conversations on platforms like LinkedIn can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your experience with batch release processes and quality assurance during interviews. Be ready to share specific examples of how you've ensured GMP compliance and handled inspections, as this will highlight your expertise.
✨Tip Number 4
Showcase your ability to work independently in a remote setting by sharing past experiences where you successfully managed projects or tasks without direct supervision. This will reassure potential employers of your self-motivation and reliability.
We think you need these skills to ace Qualified Person - Pharmaceuticals - Remote Working
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Qualified Person as outlined in the job description. Familiarise yourself with EU GMP and UK regulatory standards to demonstrate your knowledge in your application.
Tailor Your CV: Highlight your relevant experience, especially any previous roles where you acted as a Qualified Person or worked under an MIA licence. Emphasise your understanding of GMP and your ability to work independently in a remote setting.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the pharmaceutical industry. Mention specific experiences that align with the key responsibilities, such as batch release processes and collaboration with quality assurance teams.
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 for a role in pharmaceuticals.
How to prepare for a job interview at Smart4Sciences
✨Understand the Regulatory Framework
Make sure you have a solid grasp of the EU GMP and UK regulatory standards. Be prepared to discuss how your experience aligns with these regulations, as this will demonstrate your suitability for the role.
✨Showcase Your Experience
Highlight any previous roles where you acted as a Qualified Person or were involved in batch release processes. Specific examples of your contributions to quality assurance and compliance will make you stand out.
✨Emphasise Communication Skills
Since the role involves collaboration with various teams, be ready to discuss how you effectively communicate and work with others, especially in a remote setting. Share examples of successful cross-functional projects you've been part of.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills and decision-making abilities in real-world scenarios. Think about past challenges you've faced in quality assurance and how you resolved them, particularly in relation to GMP compliance.
