Are you passionate about Documentation within the Medical Device Industry? Are you also interest in working with an amazing company that offers great opportunities? Well I have the right job for you! My client is now looking to hire a Doc Control Specialist. This person will be very experience with Engineering Change Orders, Manufacturing Change Requests, Deviation, and Documentation Life Cycle. The role is a 6 months contract with the possibility to be hired on permanently.
The Doc Control Specialist requires everything from maintaining/improving the engineering documentation systems while meeting cGMP and GDP standards.
Among others, the Doc Control Specialist will have the following responsibilities:
- Engineering Change Orders
- Manufacturing Change Request
The most desirable candidates will possess the following qualifications:
- 3+ years Doc Control within Medical Device
- Knowledgeable with cGMP, GDP, ISO 9001, and ISO 13485
- Excellent reading, writing, communication, and organizational skill
This is a wonderful opportunity to join a medical device company that offers great development.
If you are interesting in the Doc Control Specialist opportunity, please forward your current resume and/or contact me on the details below!
Sthree US is acting as an Employment Business in relation to this vacancy.