At a Glance
- Tasks: Lead the production of radiopharmaceuticals and ensure compliance with GMP standards.
- Company: Join a cutting-edge PET imaging centre at Cardiff University, focused on clinical innovation.
- Benefits: Enjoy 45 days annual leave, a pension scheme, and opportunities for professional development.
- Why this job: Be part of a dynamic team making a real impact in medical imaging and patient care.
- Qualifications: Degree in a relevant scientific field and substantial GMP experience required.
- Other info: Full-time role with occasional early starts and Saturday work; diversity and inclusion are valued.
The predicted salary is between 35400 - 39600 £ per year.
Managerial, Professional and Specialist Staff – MPSS Senior Radiopharmaceutical Scientist Wales Positron Emission Tomography Imaging Centre (PETIC) Clinical Innovation Hub – School of Medicine The Wales Research and Diagnostic PET Imaging Facility is a state-of-the-art PET centre, fully equipped with a cyclotron and GMP and R&D radiochemistry facilities to produce both established and new GMP grade PET radiotracers for clinical use. We have a rare and exciting opportunity for an enthusiastic, highly motivated, and technically-minded individual with an ambition to take a lead role in our team of experts, who produce radiopharmaceuticals to Good Manufacturing Practices (GMP) standards in a purpose-designed GMP manufacturing facility. This role involves being a key member of PETIC’s GMP Production Team, responsible for providing first-line technical support for maintenance, troubleshooting, and repair of critical equipment and utilities infrastructure. You will perform equipment and process validation for F-18 radiopharmaceutical production and dispensing, including protocol preparation and execution, and providing professional guidance to the team. This position offers a platform to utilize your technical expertise and regulatory knowledge to plan and deliver small-scale projects, resolve complex issues, and minimize downtime of cleanroom facilities. You will work closely with the Head of Radiopharmacy Production and be involved in staff training, GMP standards compliance, equipment and laboratory maintenance, validation, environmental monitoring, and stock control. Additionally, you will participate in production, dispensing, and quality control of radiopharmaceuticals, operating automated and manual radiochemical synthesis with accuracy. If you wish to learn more, please contact Syed Bukhari at 02920 742005 or via email at BukhariS4@cardiff.ac.uk. This full-time (35 hours/week), fixed-term role for 3 years is based at Heath Park, Cardiff, with options for secondment. Salary ranges from £40,497 to £45,413 per annum (Grade 6). The working hours typically start between 07:00 and 09:00, with occasional early starts as early as 4:00 am, and some Saturday work on a rota basis. Cardiff University offers excellent benefits, including 45 days annual leave, pension scheme, cycle-to-work, annual pay increments, and more. We are committed to diversity and inclusion and welcome applications from all backgrounds. Key Duties include: Leading investigations and troubleshooting of PETIC’s F-18 tracer production facility. Planning and delivering small-scale process improvement projects. Risk assessing GMP production issues and proposing solutions to minimize downtime. Executing maintenance and repairs of GMP equipment and utilities. Leading investigations into GMP production issues. Performing equipment and process validation, including protocol development and execution. Building relationships with internal and external stakeholders. Training and developing GMP production staff, ensuring compliance with procedures and regulations. GMP-compliant production, storage, and transportation of PET radiopharmaceuticals. Reviewing and improving SOPs, work instructions, and policies. Participating in deviation, CAPA, and change control processes. Managing equipment calibration, validation, and maintenance schedules. Supporting environmental monitoring and incoming material testing. Performing administrative duties and leading the team to address challenges positively. Handling dangerous goods shipments following ADR regulations. Maintaining continuous professional development in GMP radiopharmaceuticals and aseptic manufacturing. Manufacturing radiopharmaceuticals in compliance with licensing and quality systems. Cleaning and maintaining cleanrooms and equipment. Person Specification – Essential Criteria: Degree/NVQ 4 or equivalent in a relevant scientific discipline. Substantial GMP aseptic pharmaceutical or radiochemistry experience, including operating automated/remotely operated equipment and troubleshooting. Experience developing new processes and procedures. Strong report writing, verbal communication, and complex information dissemination skills. Ability to explore customer needs and adapt services accordingly. Meticulous attention to detail. Problem-solving skills, initiative, and creativity. Ability to work independently, plan, and prioritize. Experience in F-18 PET Radiopharmacy and knowledge of isolator and cleanroom technology. High-level mechanical, electrical, or control systems knowledge. Fluency in Welsh, written and oral. Additional Information: Assist in audits and regulatory inspections. Maintain stock levels and clean storage areas. Operate the cyclotron particle accelerator. General Duties: Deputize for the Head of Radiopharmacy Production. Ensure confidentiality and adherence to health, safety, and equality policies. Perform other duties as required. Act as Radiation Protection Supervisor, ensuring radiation safety compliance. Participate in GMP production operations, including weekends and out-of-hours as needed. Handling ionising radiation sources requires manual dexterity, use of remote manipulators, and working in radiation-controlled areas with appropriate safety measures. #J-18808-Ljbffr
Senior Pharmaceutical Scientist employer: Cardiff University
Contact Detail:
Cardiff University Recruiting Team
BukhariS4@cardiff.ac.uk
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Pharmaceutical Scientist
✨Tip Number 1
Network with professionals in the radiopharmaceutical field. Attend industry conferences or seminars where you can meet experts and learn about the latest trends and technologies. This can help you gain insights into the role and potentially get a referral.
✨Tip Number 2
Familiarise yourself with GMP standards and regulations specific to radiopharmaceuticals. Understanding these guidelines will not only prepare you for the role but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your experience with F-18 PET Radiopharmacy in detail. Be ready to share specific examples of how you've handled troubleshooting, process validation, and equipment maintenance in previous roles.
✨Tip Number 4
Showcase your leadership skills by discussing any past experiences where you trained or developed team members. Highlighting your ability to lead investigations and improve processes will make you stand out as a candidate.
We think you need these skills to ace Senior Pharmaceutical Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in GMP aseptic pharmaceutical or radiochemistry. Emphasise your technical skills, especially in operating automated equipment and troubleshooting, as these are crucial for the role.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the position and the opportunity to lead a team in producing radiopharmaceuticals. Mention specific projects or experiences that demonstrate your problem-solving skills and attention to detail.
Highlight Relevant Qualifications: Clearly state your degree or NVQ 4 in a relevant scientific discipline. If you have experience in F-18 PET Radiopharmacy or knowledge of cleanroom technology, make sure to include this information prominently.
Showcase Communication Skills: Since strong report writing and verbal communication skills are essential, consider including examples of how you've effectively communicated complex information in previous roles. This will help demonstrate your ability to build relationships with stakeholders.
How to prepare for a job interview at Cardiff University
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with GMP standards and radiopharmaceutical production. Highlight specific projects where you led troubleshooting or process improvements, as this role requires a strong technical background.
✨Demonstrate Leadership Skills
Since the position involves training and developing staff, share examples of how you've successfully led teams or mentored colleagues in previous roles. This will show your capability to take on a managerial role within the team.
✨Prepare for Problem-Solving Scenarios
Expect questions that assess your problem-solving skills, especially related to GMP production issues. Think of complex challenges you've faced and how you resolved them, as this will demonstrate your initiative and creativity.
✨Familiarise Yourself with Regulatory Compliance
Understand the key regulations and compliance requirements in the pharmaceutical industry, particularly those related to radiopharmaceuticals. Being able to discuss these confidently will show your commitment to maintaining high standards in production.