At a Glance
- Tasks: Design and test innovative drug delivery devices in a collaborative engineering team.
- Company: Leading company in medical device development with a focus on innovation.
- Benefits: Competitive pay, hands-on experience, and a chance to impact healthcare.
- Other info: Exciting R&D environment with opportunities for professional growth.
- Why this job: Join a dynamic team and contribute to life-changing medical technologies.
- Qualifications: Degree in Engineering or related field; experience in medical devices preferred.
The predicted salary is between 21 - 21 £ per hour.
- £21.00 per hour PAYE (37 hours per week)
- We're recruiting for a
Senior Associate Device Engineer to support the development and evaluation of innovative drug delivery devices within a multidisciplinary engineering team.
This is an excellent opportunity for an engineer with experience in medical devices, drug delivery systems or combination products to work on the testing, analysis and verification of devices such as syringes and cartridges throughout the product development lifecycle.
Key responsibilities
- Design and execute mechanical and functional testing of drug delivery devices.
- Develop test methods, experimental rigs and laboratory test setups.
- Support design verification and validation activities.
- Analyse experimental data using statistical techniques and Design of Experiments (DOE).
- Contribute to risk management activities, including FMEA.
- Support design control documentation and technical reporting.
- Work closely with design, quality, regulatory, human factors and formulation teams.
- Ensure laboratory activities are carried out in accordance with ISO 13485 and established quality procedures.
About you
- Degree or HND in Mechanical Engineering, Biomedical Engineering or a related Engineering/Science discipline.
- Experience within the medical device, pharmaceutical or drug delivery sector.
- Knowledge of design verification, device testing and analytical test methods.
- Familiarity with ISO 13485, design controls and risk management (FMEA).
- Experience using CAD software (Creo preferred).
- Strong analytical and problem-solving skills with a hands‑on approach to engineering.
If you're looking for your next contract opportunity within a collaborative R&D environment and have experience developing or testing regulated medical devices, we'd love to hear from you.
Apply today with your CV, or get in touch for more information.
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Senior Associate Device Engineer in Peterborough employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the vibrant streaming and entertainment sector. Employees benefit from immediate project impact opportunities, comprehensive training, and career growth in a cloud-oriented environment, making it an ideal place for those looking to advance their skills in data engineering while working with cutting-edge technologies.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Associate Device Engineer in Peterborough
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Cpl Life Sciences.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Cpl Life Sciences is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior Associate Device Engineer in Peterborough
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 Cpl Life Sciences!
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 Cpl Life Sciences that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Cpl Life Sciences!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Cpl Life Sciences, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Cpl Life Sciences
✨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 Cpl Life Sciences 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.
✨Know Their Products
Take some time to familiarise yourself with Cpl Life Sciences’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.