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- Tasks: Lead batch release processes and ensure compliance with quality standards.
- Company: Join a top European specialty pharmaceutical company making a difference in healthcare.
- Benefits: Enjoy a competitive salary, bonus, car allowance, and flexible work options.
- Why this job: Be part of a dynamic team driving quality culture in a fast-paced environment.
- Qualifications: Must have 2+ years as a Qualified Person in the pharmaceutical industry.
- Other info: This role is based in East London/Essex, requiring on-site presence 4 days a week.
The predicted salary is between 72000 - 108000 £ per year.
Location: East London/Essex, UK – 4x a week on site, 1-day WFH
Remuneration: Up to £90,000 + 10% Bonus + Car Allowance
My client is a leading European specialty pharmaceutical company that is seeking an experienced Qualified Person. This pivotal role involves supporting the batch release of products manufactured on the business's site and driving a quality culture across the organisation. Requiring an experienced QP to join the team with prior experience working on site as a Qualified Person and ideally working on sterile and non-sterile products.
Key Responsibilities:- Oversee batch release processes to ensure compliance with regulatory standards.
- Provide QA support to manufacturing, packaging and supply chain, and to all business areas.
- Provide advice, guidance, support and mentoring to all staff with the site in matters relating to the safety, quality and efficacy of the manufacturing and distribution of medicinal products and investigational medical products.
- Review, assess and management of quality risk.
- Collaborate with cross-functional teams to maintain high-quality standards.
- Implement and promote a strong quality culture within the organization.
- To ensure product is made in accordance with manufacturing licenses and equivalent marketing authorizations.
- Assure product, process and facilities comply with national and global regulatory requirements in alignment to the site policies.
- Provide quality oversight of all activities on site and of subcontractors.
- To actively participate in/chair Site Quality Review Team Meetings.
- To ensure any significant quality or compliance issues are escalated to senior management.
- To review and approve quality documentation.
- Proven experience as a Qualified Person (Minimum 2 years as a QP) in the pharmaceutical industry.
- In-depth knowledge of regulatory requirements and quality assurance.
- Strong analytical and problem-solving skills.
- Registered UK/EU Qualified person with relevant experience in the pharmaceutical industry.
- Passionate leader able to drive a culture with Quality at the centre of decision making.
- Enjoy a fast-paced environment and autonomy.
- Strong GMP background and related decision-making skills.
- Experience working with solid dosage forms including tablet formations, capsules and non-sterile liquids and suspensions.
- Previous experience working on-site as a QP.
This role does not offer sponsorship, so you MUST have the full right to work in the UK.
Qualified Person (QP) employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP)
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. Attend industry events or join relevant online forums to connect with potential colleagues and learn about job openings.
✨Tip Number 2
Stay updated on the latest regulatory changes and quality assurance practices in the pharmaceutical sector. This knowledge will not only enhance your expertise but also demonstrate your commitment to maintaining high-quality standards during interviews.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven a quality culture in previous roles. Highlight your leadership skills and ability to mentor others, as these are key attributes for the Qualified Person position.
✨Tip Number 4
Familiarise yourself with the company’s products and their manufacturing processes. Showing that you understand their operations and challenges can set you apart from other candidates during the interview process.
We think you need these skills to ace Qualified Person (QP)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person, particularly focusing on your work with sterile and non-sterile products. Use specific examples to demonstrate your compliance with regulatory standards and your contributions to quality assurance.
Craft a Compelling Cover Letter: In your cover letter, express your passion for quality assurance in the pharmaceutical industry. Mention your leadership skills and how you can drive a quality culture within the organisation. Be sure to relate your previous experiences directly to the responsibilities outlined in the job description.
Highlight Relevant Qualifications: Clearly state your qualifications, including your registration as a UK/EU Qualified Person. Emphasise your analytical skills and any specific training or certifications that are relevant to the role, especially those related to GMP and quality risk management.
Proofread Your Application: Before submitting your application, thoroughly proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at JR United Kingdom
✨Know Your Regulatory Standards
Make sure you have a solid understanding of the regulatory requirements relevant to the pharmaceutical industry. Be prepared to discuss how you've ensured compliance in your previous roles, especially regarding batch release processes.
✨Showcase Your Quality Culture Experience
Highlight any initiatives you've led or participated in that promoted a quality culture within your previous organisations. This could include training sessions, mentoring staff, or implementing new quality assurance practices.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to manage quality risks. Prepare examples from your past experience where you successfully navigated challenges related to product safety, quality, or compliance.
✨Demonstrate Cross-Functional Collaboration
Be ready to discuss your experience working with cross-functional teams. Provide examples of how you've collaborated with manufacturing, packaging, and supply chain teams to maintain high-quality standards and resolve issues.
