Opeyemi Babalola

· Responsible for removing burrs, sharp edges, and imperfections from metal and composite materials using various deburring tools.

· Responsible for inspection of finished parts to ensure all burrs and sharp edges are removed and verify that the parts meet engineering specifications and quality standards.

· Ensuring that all parts meet industry’s tolerance and safety standards.

· Select and operate appropriate deburring tools, including manual hand tools, power tools, passivation machine, grinders, etc. depending on part requirements.

· Maintain accurate records of completed work, including inspection results, part counts, and any issues that arise during the deburring process.

· Effective use of CDT Epicor software for tracking operations, reporting processes, and updating activities during deburring and passivation processes.

· Adhere to all safety protocols and maintain a clean, safe, and organized work environment.

· Work with production, engineering, and quality control teams to address any issues related to deburring and contribute to continuous improvement initiatives.

· Worked with R&D engineers to design and build prototypes.

· Maintains proper documentation of calibrations, periodic safety inspections, and preventive maintenance procedures during project designs.

· Worked with R&D engineers to develop basic processes needed for production fabrication.

· Worked with technicians and engineers to create documentation for the processes used in building products.

· Conduct product evaluations on prototypes and address customer concerns.

· Worked with engineers and technicians in product change requests and ensure adherence to quality standards.

· Assembled medical products and devices such as Talisman, Amplatzer Septer Occluders, Amplatzer Duct Occluders, etc using tools and equipment such as microscope and specialized hand tools to assemble components and attached labels.

· Performed quality control checks including visual inspections or using specialized equipment to test products.

· Maintained a clean and organized work area, adhering to all safety and quality regulations and procedures and wearing personal protective equipment (PPE) including gowns, masks, gloves, and hairnets.

· Followed written instructions, procedures, diagrams, and verbal instructions such as Good Manufacturing Practices (GMP) and ISO regulations.

· Reported non-conformance issues to management through the supervisor for resolution.

· Learnt and adhered to safety policies and procedures in the medical device industry.

· Worked with Oxyl-Fusion team to meet up with daily, weekly, and monthly goals.

· Padding and un-padding of Centrifuge devices.

· Responsible for quality and adheres to manufacturing processes requirements during production.

· Built products by following all processes according to Standard Operating Procedures.

· Maintained accurate records including hourly, daily, and weekly production targets.