Job Opportunity
We are seeking an ambitious and detail-oriented individual to join our team in developing Standard Operating Procedures (SOPs) for medical device production. The ideal candidate will have a strong background in Industrial Engineering and Management, Quality Engineering or similar field.
The selected candidate will be responsible for analyzing and mapping existing production workflows, collaborating with quality and production teams to develop SOPs, writing and formatting SOPs aligned with ISO 13485 and GMP requirements, supporting operator training and implementation of SOPs, and contributing to continuous improvement and audit readiness.
* Responsibilities:
* Analyze and map existing production workflows
* Develop SOPs in collaboration with quality and production teams
* Write and format SOPs aligned with regulatory requirements
* Support operator training and implementation of SOPs
* Contribute to continuous improvement and audit readiness
Requirements
* Education:
* Bachelor's or Master's degree in Industrial Engineering and Management, Quality Engineering or similar
Benefits
* Monthly stipend supported by IEFP
* Meal allowance
About the Role
This is a fantastic opportunity to gain experience in regulated industries, work in a real-world, production-floor environment, receive direct mentorship and technical training, and build your professional network. You'll also have the chance to contribute to the development of quality standards and regulatory compliance in medical device manufacturing.
If you're passionate about quality, safety, and innovation in healthcare, we encourage you to apply for this exciting opportunity. Send us your CV and tell us why you're excited to join our team.