Back to Job SearchWe are recruiting a Medical Devices Engineer to join a leading Pharmaceutical company in the Walloon Region, Belgium. As the Medical Device Engineer, you will play a crucial role in translating complex technical information into clear, compliant documentation for Drug delivery / autoinjector portfolio.
This mission can be offered remotely across Europe for the right candidate.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Medical Device Engineer will be varied; however, the key duties and responsibilities are as follows:
- Author, update, and maintain risk management documentation for autoinjectors and safety syringes, ensuring technical accuracy and consistency.
- Perform detailed checks for consistency, completeness, and traceability across risk management files and design control records.
- Collaborate with cross-functional teams to collect and consolidate technical inputs, facilitating risk documentation review meetings.
- Contribute to the development of templates and practices for risk management documentation, supporting continuous improvement initiatives.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Medical Device Engineer, we are looking to identify the following on your profile and past history:
- Relevant degree in Engineering, Life Sciences, Pharmaceutical Sciences, Technical Writing, or a related discipline.
- Extensive industry experience in medical devices, drug-device combination products, or regulated documentation.
- A working knowledge and practical experience with ISO 14971 risk management principles and autoinjector development.
This role is perfect for someone who thrives in a structured environment and enjoys ensuring that documentation is technically sound and aligned with regulatory standards. You will be working closely with Device SMEs, Quality, Safety, Regulatory, and Project stakeholders, ensuring that all risk management files and related design control documentation are well-structured and aligned with project timelines.
Key Words: Medical Device Engineer / Technical Writing / Risk Management / Autoinjectors / Safety Syringes / ISO 14971 / Design Control / Regulatory Compliance / Medical Devices / Drug-Device Combination Products / Drug Delivery / Autoinjector
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.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
