An exciting role awaits for a Senior Associate Device Engineer to join a leading company in the pharmaceutical industry based in Cambridgeshire, UK. As the Senior Associate Device Engineer, you will be at the forefront of innovative drug delivery device development, ensuring that cutting-edge technology meets the highest standards of quality and performance.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Associate Device Engineer will be varied however the key duties and responsibilities are as follows:
1. As the Senior Associate Device Engineer, you will collaborate with multidisciplinary teams to assess and investigate performance factors of drug delivery devices.
2. As the Senior Associate Device Engineer, you will support the project lead in authoring, reviewing, and managing design control documentation.
3. As the Senior Associate Device Engineer, you will engage with external vendors and internal partners for design assessment, verification, and manufacturing process qualification.
4. As the Senior Associate Device Engineer, you will develop test methods, experimental rigs, and setups to ensure robust device performance.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Senior Associate Device Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree in Engineering or a related Science subject.
2. Proven industry experience in device control system life cycle and device testing.
3. A working knowledge and practical experience with mechanical and/or electronic testing of drug delivery devices.
Key Words:
Engineering / Technologist / Medical Devices / Combination Products / Drug Delivery Devices / Device Engineering / Design Control / Design Control Documentation / Design Verification / Design Validation / Device Development / Product Development / Device Testing / Mechanical Testing / Electronic Testing / Test Method Development / Test Method Validation / Engineering Assessment / Risk Management / Risk Mitigation / dFMEA / uFMEA / Failure Mode Analysis / Human Factors Engineering / Usability Studies / Design Assurance / Specification Development / Specification Setting / Analytical Method Development / Experimental Design / Design of Experiments (DOE) / Statistical Analysis / Data Analysis / Data Management / Technical Documentation / ISO 13485 / Quality Systems / GMP / GLP / Medical Device Regulations / Combination Device Products / Manufacturing Process Qualification / Supplier Management / Vendor Management / Laboratory Testing / Engineering Calculations / Free Body Diagrams / Beam Bending / Friction Analysis / CAD / Creo / Product Performance Testing / Root Cause Analysis / Troubleshooting / Verification Testing / Stability Testing / Transportation Testing / Scientific Reporting / Validation Protocols / Laboratory Equipment / Metrology / Compliance / Pharmaceutical Industry / Life Sciences / Device Centre of Excellence / Cross-Functional Collaboration
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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