Associate Quality Assurance Engineer - Nights
Perrigo Company plc
6 hours ago
On-site
Eau Claire, WI
Operations
Description Overview
As a Quality Assurance Engineer, you will support and participate in continuous improvement activities in the operations areas and perform professional analytical support work in the Quality arena to support operational processes.
This position works autonomously under the supervision of the Factory Quality Manager.
Please note: 2-2-3 rotation working from 6pm - 6:10am.
Scope of the Role
- Lead/participate in quality-driven initiatives supporting continuous Quality improvements using data analysis techniques and other improvement tools.
- Review and approve documents including deviations, Annual product reports, non-routine batch status change requests, planned deviations, and calibration non-conformances.
- Provide initial risk assessment of Quality events.
- Work with operations, laboratory, engineering, and maintenance teams to develop, evaluate, and implement action plans to maintain or improve product and process quality.
Experience Required
- Bachelor’s degree in a scientific discipline or closely aligned field; minimum two years’ experience working in an FDA-regulated industry (preferred).
- Demonstrated understanding and application of Continuous Improvement and Root Cause analysis skills.
- Demonstrated understanding of and ability to apply cGMPs and U.S. FDA laws and requirements in an FDA-regulated industry.
- Strong functional knowledge of SAP systems.
- Ability to organize multiple tasks, manage changing priorities, and meet project deadlines.
Benefits
- Competitive compensation; benefits tailored to supporting you and your family; career development opportunities (including information via “Total Rewards”).
Application Instructions
- To apply, click the APPLY button at the bottom of the application (SAVE only saves your profile and does not submit the application).
As a Quality Assurance Engineer, you will support and participate in continuous improvement activities in the operations areas and perform professional analytical support work in the Quality arena to support operational processes.
This position works autonomously under the supervision of the Factory Quality Manager.
Please note: 2-2-3 rotation working from 6pm - 6:10am.
Scope of the Role
- Lead/participate in quality-driven initiatives supporting continuous Quality improvements using data analysis techniques and other improvement tools.
- Review and approve documents including deviations, Annual product reports, non-routine batch status change requests, planned deviations, and calibration non-conformances.
- Provide initial risk assessment of Quality events.
- Work with operations, laboratory, engineering, and maintenance teams to develop, evaluate, and implement action plans to maintain or improve product and process quality.
Experience Required
- Bachelor’s degree in a scientific discipline or closely aligned field; minimum two years’ experience working in an FDA-regulated industry (preferred).
- Demonstrated understanding and application of Continuous Improvement and Root Cause analysis skills.
- Demonstrated understanding of and ability to apply cGMPs and U.S. FDA laws and requirements in an FDA-regulated industry.
- Strong functional knowledge of SAP systems.
- Ability to organize multiple tasks, manage changing priorities, and meet project deadlines.
Benefits
- Competitive compensation; benefits tailored to supporting you and your family; career development opportunities (including information via “Total Rewards”).
Application Instructions
- To apply, click the APPLY button at the bottom of the application (SAVE only saves your profile and does not submit the application).