Title: QA Specialist II
Location: Austin, TX
Duration: 16 Months + Possible extension
Important Note: PLEASE BE INFORMED THAT CANDIDATE WHEN THEY START, THEY WILL BE WORKING A REGULAR WORK SCHEDULED (MONDAY TO FRIDAY) TO TRAIN FOR ABOUT 6 TO 8 WEEKS THEN THEY WILL MOVE TO THE WEDNESDAY to SATURDAY 8 AM TO 6 PM.
Job Responsibilities
- Employee must be able to work onsite during these hours.
- This position will support 3rd party for medical devices, device history records and mostly will handle batch Records.
- Must have Bachelor’s degree preferably in STEM Engineering / Science degrees are best fits
- 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 non conformances 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.
Top 3 Skills
- Ability to follow procedures
- Strong attention to detail
- Strong understanding of med device quality docs.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.