Quality Systems Specialist (GMP Document Review)

We are currently seeking a Quality Systems Specialist (GMP Document Review) for a prominent Medical Device client of ours. This position is in Rocklin, CA. Details for the position are as follows :

Job Description :

• Pay : 25.00-27.00 / hr.
• Length of Assignment : Immediate need. Contract through Feb 2026.
• 100 percent onsite position.
• At least 1 year of experience reviewing docs in a GMP regulated setting OR experience working in a quality role in a GMP regulated setting.
• Will be part of the Quality team and responsible for providing quality support for the site quality management system.
• This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD / IVDR, CFR 21, GxP, and the quality manual.
• Experience reviewing documentation (i.e., DHF, DHR, MDF, ISO 13485, etc..) is a plus, but not required.
• Responsible for the analysis, development, and operation of quality and risk management systems.
• Activities include developing standards for quality, documentation, and processes as well as continuous improvement and preventive activities.