About Us
At {company}, we are 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, nutritionals, and branded generic medicines.
Salary: $100,000 - $120,000 per year
Main Responsibilities:
* Identify manufacturing process defects by dispositioning non-conforming material, identifying primary root causes, and suggesting corrective and preventative actions.
* Assist in the development of product quality plans, documents, and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, and Failure Mode Effect Analysis (FMEA) in conjunction with other product development team members.
* Become skilled at using process monitoring systems by starting to identify critical process steps and applying basic methods to reduce process variation to eliminate the cause of defects.
* Assist product/process improvement efforts by systematically gathering quality metric data based on previous program templates and by assisting in the appropriate analysis methods to enhance sustaining product design and new product development.
* Become skilled at using quality tools and training materials by working with existing quality tools and training materials and by understanding the evolution/history of tools in use.
* Participate in validation activity, including providing input to owning activities such as protocol/report writing and managing execution of validation activities.
* Participate in corrective and preventive action activity.
* Participate in Field Discrepancy Notification (FDN) investigations.
Education & Experience:
* National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline.
* 2+ years of related work experience, or an equivalent combination of education and work experience.