What are the responsibilities and job description for the Quality Assurance Medical device position at Infoway Solutions LLC?
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
- Recent graduates encouraged to apply.
- 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 Type: Contract
Pay: $21.02 - $22.15 per hour
Expected hours: 40 per week
Benefits:
- Health insurance
- Paid time off
Schedule:
- 8 hour shift
- Day 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: 2 years (Preferred)
Ability to Commute:
- Sturtevant, WI 53177 (Required)
Ability to Relocate:
- Sturtevant, WI 53177: Relocate before starting work (Required)
Work Location: In person
Salary : $21 - $22
