At a Glance
- Tasks: Lead exciting projects in nuclear medicine, ensuring successful implementation and customer satisfaction.
- Company: Join a market-leading company in radiopharmacy with a focus on innovation.
- Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
- Other info: Frequent travel and opportunities for career growth in a collaborative environment.
- Why this job: Make a real impact in healthcare by overseeing cutting-edge technology in radiopharmaceuticals.
- Qualifications: Experience in PET/SPECT production and knowledge of regulatory compliance required.
The predicted salary is between 50000 - 65000 £ per year.
This role is a full‑time, office‑based position. However, the role involves frequent travel to our customer sites both in the UK and internationally. As a Project Lead, you will oversee projects for our market‑leading nuclear medicine LIMS (Laboratory Information Management System), PETra and SPECTra. The ideal candidate will have a background in PET/SPECT production and be familiar with regulatory compliance. This is a customer‑facing role with a high level of interaction to advise on numerous technical aspects with respect to implementation, processes and applications.
Responsibilities
- Take ownership of project delivery, including scope, timelines, and risks, while coordinating cross‑functional teams and acting as the primary customer contact.
- Own and lead the end‑to‑end validation lifecycle including Validation Planning, IQ, OQ, and support of PQ activities.
- Develop, review, and maintain validation documentation.
- Act as Subject Matter Expert (SME) for PETra and SPECTra, providing configuration expertise, best practice guidance, and support for pre‑sales activities and solution design.
- Liaise with application developers to drive product improvements and ensure alignment between customer needs and product capability.
- Provide SME support for customer audits and inspections.
- Deliver training, prepare materials and provide ongoing coaching to new customers as part of a newly installed system.
- Support User Acceptance Testing, post‑install validation, including helpdesk support where requested.
- As SME, test and approve updated applications during the release process, taking ownership of customer upgrades, including on‑site software testing where required.
Additional Duties
- Support sales team in application demonstrations.
- Bid process, tender document review.
- SME support for specific technical questions.
- Attend commercial conferences and user group meetings.
- Presentation requirements for group/users as directed.
- Company SME for guide, advise and update colleagues on best processes and practices within Nuclear Medicine.
The above list is not exhaustive and, as such, you may be required to undertake other duties as appropriate.
Requirements
Essential
- In‑depth knowledge of radiopharmaceutical production processes.
- Understanding of GMP and regulatory environments (GAMP 5, Annex 11, 21 CFR Part 11 knowledge).
- Ability to work with end users on‑site to ensure successful deployments, training and ultimately customer satisfaction.
- Ability to work with the internal development and QA teams to help drive future developments.
- Ability to enhance and maintain training materials.
- Experience delivering basic and/or advanced training.
- Ability to understand and work with IT teams at customer facilities.
Radiopharmacy Project Lead - UK (Sheffield based) employer: LabLogic FR
As a leading employer in the radiopharmacy sector, we offer a dynamic work environment in Sheffield that fosters innovation and collaboration. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for international travel, allowing you to expand your expertise while working on cutting-edge nuclear medicine projects. Join us to be part of a supportive culture that values your contributions and prioritises customer satisfaction.
StudySmarter Expert Advice🤫
We think this is how you could land Radiopharmacy Project Lead - UK (Sheffield based)
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We think you need these skills to ace Radiopharmacy Project Lead - UK (Sheffield based)
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at LabLogic FR!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show LabLogic FR that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at LabLogic FR
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at LabLogic FR that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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