San Antonio, TX
The client is a Medical Device contract manufacturer of a number of different implantable products. They manufacture a number of Class I, II and III Medical Devices. They are in need of a Technical Writer to support their manufacturing group. They will be working with the manufacturing team, gathering requirements from the client and writing SOP’ s for the project.
Day to Day Responsibilities:
This consultant will be responsible for writing technical documents for the client’ s manufacturing team. This individual will be responsible for gathering the requirements that need to be put into SOP’ s, and creating the documentation from there.
This consultant will be supporting the manufacturing and process teams primarily. They should come from a Medical Device Manufacturing background with an understanding of GMP and FDA compliance requirements. This business unit utilizes a lot of Injection Molding during their manufacturing processes, so someone with that experience will be preferred.
· Medical Device: 3-5 years
· Technical Writing: 3-5 years
· Writing Manufacturing SOP’ s: 3-5 years
· GMP: 3-5 years
· Injection Molding