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- Tasks: Lead projects to enhance healthcare quality and access, ensuring compliance and effective regulation.
- Company: Join the Medicines and Healthcare products Regulatory Agency, making a difference in public health.
- Benefits: Competitive salary, flexible hybrid working, and opportunities for professional growth.
- Other info: Dynamic role with a focus on collaboration and innovation in healthcare.
- Why this job: Make a real impact on healthcare by driving quality and access initiatives.
- Qualifications: Project management experience and strong communication skills required.
The predicted salary is between 68422 - 68422 £ per year.
We are currently looking for a Project Manager to join our Product Information Quality Unit Function within the Healthcare Quality & Access group. This is a full-time opportunity, on a one year fixed term contract/loan/internal move or temporary promotion basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU.
Government departments and agencies are working towards implementing a minimum 60% attendance in office sites. We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 12 days a month, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly.
The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research. The objective of the Healthcare Quality and Access portfolio is to drive quality and critically appraise benefits and risks to inform robust decisions on healthcare access including accelerated access pathways. It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable licensing and market access, as well as ensuring compliance with regulations and standards.
The Authorisation Lifecycle function is an enabler, central to delivery of the frontline HQA group. It includes data assurance and quality, high-volume certification work, and support to the frontline functions. It also includes some more complex activity that supports across the product lifecycle.
PIQU Project Manager - £68,422 p.a. + benefits in London employer: Medicines and Healthcare Products Regulatory Agency
Contact Detail:
Medicines and Healthcare Products Regulatory Agency Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land PIQU Project Manager - £68,422 p.a. + benefits in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at the Medicines and Healthcare products Regulatory Agency. A friendly chat can open doors and give you insider info that could make all the difference.
✨Tip Number 2
Prepare for the interview by researching the company’s recent projects and initiatives. Show us that you’re not just interested in the role but also passionate about what we do in enhancing healthcare quality and access.
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. We want to hear about your past experiences and how they relate to the PIQU Project Manager role, so be ready to share specific examples of your achievements.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression and shows us that you’re genuinely interested in joining our team.
We think you need these skills to ace PIQU Project Manager - £68,422 p.a. + benefits in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the PIQU Project Manager role. Highlight relevant experience and skills that match the job description. We want to see how you can bring value to our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about this role and how your background aligns with our mission at StudySmarter. Keep it engaging and personal.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples to demonstrate how you've made an impact in previous roles. We love seeing results and how you’ve contributed to success.
Apply Through Our Website: We encourage you to apply through our website for a smooth application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency
✨Know Your Stuff
Make sure you understand the role of a PIQU Project Manager and the specific responsibilities within the Healthcare Quality & Access group. Brush up on relevant regulations and standards in the healthcare sector, as well as the importance of data assurance and quality.
✨Show Your Flexibility
Since the role involves a hybrid working model, be prepared to discuss your experience with both remote and on-site collaboration. Highlight any past experiences where you successfully adapted to different working environments and how you managed to maintain productivity.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle complex situations. Think of examples from your previous roles where you had to critically appraise benefits and risks, and be ready to explain your thought process and outcomes.
✨Engage with the Interviewers
Don’t just answer questions; engage in a conversation. Ask insightful questions about the team dynamics, current projects, and how the PIQU Project Manager fits into the bigger picture. This shows your genuine interest in the role and helps you gauge if it’s the right fit for you.