In this role you will be responsible to managed SCRs (Suppliers Change Requests). You will report to Supplier Quality manager. Come strengthen your specialized skills and enhance your expertise. Well support you with the training, mentorship, guidance, and networks you need to advance, and empower you to work in the way thats best for you.
Responsibilities may include the following and other duties may be assigned:
Complete Supplier Change Control activities on time to prevent any line disruptions.
Understand and operate according to medical device regulatory guidelines (GMP, FDA, ISO13485, AIMD R-PAL) and company Quality System procedures.
Measures performance against process requirements.
Coordinate and follow up with different internal functions to ensure an on-time execution.
Communicates team progress.
Required Knowledge and Experience:
3rd or 4th year of Industrial Engineering/Quality Assurance or equivalent degree study
Proficient in English.
Good inter-personal skills - motivate without authority.
Meticulous with close attention to details.
Capabilities and desire for self-learning.
Experience in a Medical device company or Quality Assurance.
Requirements: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
This position is open to all candidates.