At a Glance
- Tasks: Write technical reports and manage stability trials for medical devices.
- Company: Leading multinational Medical Devices client based in Blackpool.
- Benefits: Gain valuable experience in a regulated industry with potential for contract extension.
- Other info: Opportunity to work in a dynamic environment with a focus on compliance.
- Why this job: Make a real impact in the medical field while developing your scientific skills.
- Qualifications: Degree in science and experience in medical devices preferred.
The predicted salary is between 30000 - 40000 £ per year.
PE Global is currently recruiting for a Stability Scientist for an initial 6-month contract role with a leading multinational Medical Devices client based in Blackpool.
Job Responsibilities:
- Write technical justifications for MDR stability programme.
- Write technical protocols and reports for shelf-life aging studies.
- Manage set-up of stability trials in collaboration with relevant departments.
- Manage samples for studies and testing.
- Support re-validation of stability environmental chambers through documentation and coordination.
- Support execution of annual stability programme.
- Co-ordinate own week to week workload in line with your project plans and departmental priorities and overall business framework.
- Collate resource hours.
- Adhere to the Change Control and Design Control requirements.
Requirements:
- Degree qualified – ideally science.
- Previous experience in medical device or related regulated industry.
Interested candidates should submit an updated CV.
Stability Scientist - MDR Compliance & Stability Programs employer: PE Global (UK)
PE Global is an exceptional employer, offering a dynamic work environment in Blackpool where innovation meets compliance in the medical devices sector. Employees benefit from a collaborative culture that prioritises professional growth and development, alongside competitive remuneration and flexible working arrangements. Join us to contribute to meaningful projects while advancing your career in a supportive and forward-thinking organisation.
StudySmarter Expert Advice🤫
We think this is how you could land Stability Scientist - MDR Compliance & Stability Programs
✨Tip Number 1
Network like a pro! Reach out to people in the medical devices field on LinkedIn or at industry events. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Show them you’re not just another candidate; you’re genuinely interested in their work and how you can contribute to their stability programmes.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to stability studies and regulatory compliance. We want you to feel confident and ready to showcase your expertise!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace Stability Scientist - MDR Compliance & Stability Programs
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in the medical device industry. We want to see how your skills align with the responsibilities of a Stability Scientist, so don’t hold back on showcasing your technical expertise!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. We love seeing enthusiasm and a clear understanding of the MDR stability programme, so let your passion show!
Be Clear and Concise:When writing your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your qualifications and experiences that relate to the job description.
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at PE Global (UK)
✨Know Your Stuff
Make sure you brush up on your knowledge of MDR compliance and stability programmes. Familiarise yourself with the technical aspects of shelf-life aging studies and be ready to discuss how you've managed stability trials in the past.
✨Showcase Your Experience
Prepare specific examples from your previous roles that highlight your experience in the medical device industry. Talk about how you've handled documentation, co-ordinated workloads, and adhered to change control requirements.
✨Ask Smart Questions
Come prepared with questions that show your interest in the role and the company. Inquire about their current stability programmes or how they manage cross-departmental collaboration. This shows you're engaged and thinking critically about the position.
✨Be Organised
Since the role involves managing your own workload, demonstrate your organisational skills during the interview. Discuss how you prioritise tasks and manage project plans effectively, ensuring you align with departmental priorities.
