At a Glance
- Tasks: Join a dynamic team to develop innovative drug delivery technologies that improve patient outcomes.
- Company: Proclinical, a leader in pharmaceutical advancements with a collaborative culture.
- Benefits: Competitive salary, opportunities for professional growth, and a chance to make a real impact.
- Other info: Flexible work environment with opportunities for travel and relocation to Cambridge.
- Why this job: Be at the forefront of engineering and science, contributing to cutting-edge healthcare solutions.
- Qualifications: Degree in Science or Engineering, experience in device testing, and strong problem-solving skills.
The predicted salary is between 40000 - 55000 £ per year.
Are you ready to use your device engineering expertise to help develop the next generation of drug delivery technologies that could improve patient outcomes worldwide?
Proclinical is seeking a Senior Associate Device Engineer to join a dynamic team in the UK. This role focuses on supporting the development and testing of innovative drug delivery devices, including components like syringes and cartridges. You will play a key role in risk assessment, experimental analysis, and ensuring compliance with quality standards. This is an excellent opportunity for someone passionate about engineering and science to contribute to cutting‑edge pharmaceutical advancements.
Responsibilities
- Collaborate with multidisciplinary teams to assess and investigate drug delivery device performance factors.
- Author, review, and manage design control documentation.
- Support interactions with external vendors and internal partners for design assessment, verification, and manufacturing process qualification.
- Develop and validate test methods, experimental rigs, and setups.
- Contribute to early‑stage usability and market research studies to identify user requirements.
- Design and evaluate test rigs and challenge parts.
- Assess supplier designs, identify critical areas, and mitigate potential failure modes.
- Conduct risk management activities, including input to dFMEA and uFMEA.
- Apply statistical and engineering expertise to solve problems and support decision‑making.
- Analyze data using statistical tools to quantify device performance and controlling parameters.
- Operate laboratory equipment and ensure compliance with SOPs and risk assessments.
- Manage ISO 13485‑related documentation, including change control and instrument compliance.
- Prepare scientific reports and ensure accurate data transcription and analysis.
- Perform additional duties as required to support business goals.
Key Skills and Requirements
- Degree or equivalent qualification in a relevant Science or Engineering discipline.
- Strong knowledge of mechanical and/or electronic testing of drug delivery devices.
- Experience in test method development, validation, and device lifecycle management.
- Familiarity with design assessment, specification setting, and analytical method development.
- Proficiency in CAD software (preferably Creo) and engineering calculations.
- Understanding of GLP/GMP, laboratory safety, and ISO 13485 standards.
- Skilled in using scientific measuring and testing equipment.
- Excellent problem‑solving, communication, and organizational skills.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Flexible, adaptable, and detail‑oriented with a commitment to quality and excellence.
- Willingness to travel or relocate to the Cambridge area if required.
Senior Associate Device Engineer employer: Proclinical Group
Proclinical Group is an excellent employer, offering a dynamic work culture that fosters collaboration and innovation in the field of diagnostic technologies. Employees benefit from comprehensive training programs, opportunities for professional growth, and the chance to make a meaningful impact on customer satisfaction and business success in the vibrant location of Croydon, UK.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Associate Device Engineer
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Proclinical Group. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
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 Proclinical Group.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Proclinical Group. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
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 Proclinical Group is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior Associate Device Engineer
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 Proclinical Group!
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 Proclinical Group 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 Proclinical Group!
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 Proclinical Group, 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 Proclinical Group
✨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 Proclinical Group that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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 Proclinical Group’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.
