No more applications are being accepted for this job
- Must have a minimum of 3 years of experience in a medical device or pharma regulated environment, preferably in manufacturing. HEAVY Documentation role doing batch review, quality doc approvals
- Documentation exp. on Resume review of quality documents batch release experience or lab notebook (design, manufacturing or release).
- Experience in nonconformances and CAPA is a plus.
- Must have strong attention to detail.
- Must know and be able to follow procedures, review document requirements and determine if acceptable for procedure and if not escalate. Internship, co-ops and schooling will not be considered.
- Masters degrees will not supplant any years of experience so must still come with minimum 3 years of experience.Top 3 Skills
- ability to follow procedures
- strong attention to detail
- strong understanding of med device quality docs.
- Manager will consider candidates who are willing to relocate at their own expense.
- Interview will be Video with Crystal .
QA Specialist II - Austin, United States - Spectraforce Technologies
Description
Job Title:QA Specialist IIJob Location:Austin, TX 73301
Job Duration: 6 months
Note : WILL BE WORKING A REGULAR WORK SCHEDULED (MONDAY THRU FRIDAY) TO TRAIN FOR ABOUT 6 TO 8WEEKS THEN THEY WILL MOVE TO THE WEDNESDAY THRU SATURDAY8 am to 6 pm (10 hours a day)
Job Description:
This position will support 3rd party for medical devices, device history records and mostly will handle Batch Records.
Skills:
Must have Bachelor's degree preferably in STEM Engineering / Science degrees are best fit