Job Description:
Job Description: This position supports a wide array of activities related to: Supplier Management
- Supplier Management Activities including: Supplier adds, supplier re-evaluations, supplier ratings, supplier corrective action management, supplier notification of change
- Adherence to regulations - Assist with adherence to all Federal, State, and Local Regulations controlling the manufacture of medical devices.
- Support the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards.
- Support the operation of the Quality System process related to Corrective/Preventive actions and product non-conformance control including: capturing data associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
Requirements:
- BS/BA in Physical Science or Engineering or 2 + years in medical device/Pharmaceutical industry
- Experience in Quality Assurance and/or other regulated industry or similar experience a plus.
- Strong technical writing skills and general problem solving skills.
- Manage multiple priorities and work with interruptions.
- GLP and/or GMP experience a plus.
- Medical Device knowledge a plus.
- Requires Vision Assessment (20/20 near visual acuity & acceptable color vision).
Work Location: 13900 Grandview Parkway, Sturtevant WI
Work Schedule: 8 am -4:30 pm with some flexibility for start time
Contact:
Mani - Team Lead HR Recruiter
Email: mani.t@infowaygroup.com
Cell: (925) 241-5753 Ext 106
Info Way Solutions LLC
“Email is the best way to reach me”
Job Types: Contract, Temp-to-hire
Pay: $23.00 - $25.70 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 10 hour shift
- 8 hour shift
- Monday to Friday
Education:
- Bachelor's (Required)
Experience:
- Quality Assurance: 2 years (Required)
- medical device/Pharmaceutical industry: 2 years (Required)
- GMP: 2 years (Preferred)
- GLP: 2 years (Preferred)
- Medical Device knowledge: 2 years (Preferred)
- FDA regulations: 1 year (Preferred)
Ability to Commute:
- Sturtevant, WI (Preferred)
Ability to Relocate:
- Sturtevant, WI: Relocate before starting work (Preferred)
Work Location: On the road