Hollister Incorporated
Plant Quality Engineer III
Hollister Incorporated, Stuarts Draft, Virginia, United States, 24477
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We Make Life More Rewarding and Dignified
Location : Stuarts Draft Department :
Salary Range varies on education and experience from $66,000- $115,000
Support the plant manufacturing facility in assuring quality products by meeting all regulatory compliance requirements of the Quality System, performing process capability studies, determining process improvements, instituting corrective action for process & Quality System deficiencies and partnering with operations in achieving both plant and GQM objectives compatible with Hollister’s Mission and Vision.
Responsibilities:
Act as Quality Resource to help facilitate completion of assigned Change Controls.
Lead and perform pFMEA and products/process qualifications.
Review, evaluate and disposition non-conforming materials.
Respond to assigned CAPAs and QNs for investigation, root cause analysis and implement solutions.
Plan, coordinate, execute and document process capability, validation studies, and process improvement studies.
Create, execute and conclude results for protocols, including final reports and summaries.
Support Operations and GQM strategic plans in leading or supporting projects.
Plan, coordinate, and document Quality Plans and work instructions.
Conduct training on defect awareness.
Work collaboratively with Value Stream Process Engineers to identify, investigate and solve quality issues.
Responsible for achieving competency in all identified skill requirements outlined in associated training profile for position.
Other duties and tasks as assigned.
Essential Functions of the Role**
Prolonged periods of sitting
Ability to interface with a computer for long periods of time
Frequent movement over large manufacturing floor areas
Occasionally move products/parts from production floor into testing area, up to 20 pounds
Ability to train/facilitate
Flexible work schedule with start/stop times across all shifts
Communication skills, both written and oral
Work Experience Requirements
Number of Overall Years Necessary: 0-5 years
Experience in Quality Engineering or equivalent industry disciplines preferred
Experience in medical device manufacturing regarding Quality System requirements per 21 CFR 820 and/or ISO 13485 preferred
Education Requirements
Bachelor’s Degree in Science (Engineering, Math, Natural Sciences, or related study preferred)
Specialized Skills/Technical Knowledge
Knowledge and application of basic statistics and experimental design preferred
Knowledge and experience in statistical software packages preferred (ex. Minitab)
Technical writing skill preferred.
Experience working with self-directed work teams preferred
Experience performing internal/external audits and evaluations preferred
Experience with product design and product design related regulatory requirements preferred
Knowledge and implementation of medical device Quality System requirements (FDA and ISO) preferred
ASQ Certified Quality Engineer preferred
Knowledge of Lean and Six Sigma Black Belt principles preferred
Basic technical writing skills required, advanced technical writing skills preferred
Knowledge of SAP/ERP Systems a plus
Knowledge of Microsoft Office Products (Word, Excel, Project, Access, PowerPoint)
Local Specifications (English and Local Language) About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.
EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job Segment:
Facilities, Technical Writer, Testing, Compliance, ERP, Operations, Technology, Legal
#J-18808-Ljbffr
We Make Life More Rewarding and Dignified
Location : Stuarts Draft Department :
Salary Range varies on education and experience from $66,000- $115,000
Support the plant manufacturing facility in assuring quality products by meeting all regulatory compliance requirements of the Quality System, performing process capability studies, determining process improvements, instituting corrective action for process & Quality System deficiencies and partnering with operations in achieving both plant and GQM objectives compatible with Hollister’s Mission and Vision.
Responsibilities:
Act as Quality Resource to help facilitate completion of assigned Change Controls.
Lead and perform pFMEA and products/process qualifications.
Review, evaluate and disposition non-conforming materials.
Respond to assigned CAPAs and QNs for investigation, root cause analysis and implement solutions.
Plan, coordinate, execute and document process capability, validation studies, and process improvement studies.
Create, execute and conclude results for protocols, including final reports and summaries.
Support Operations and GQM strategic plans in leading or supporting projects.
Plan, coordinate, and document Quality Plans and work instructions.
Conduct training on defect awareness.
Work collaboratively with Value Stream Process Engineers to identify, investigate and solve quality issues.
Responsible for achieving competency in all identified skill requirements outlined in associated training profile for position.
Other duties and tasks as assigned.
Essential Functions of the Role**
Prolonged periods of sitting
Ability to interface with a computer for long periods of time
Frequent movement over large manufacturing floor areas
Occasionally move products/parts from production floor into testing area, up to 20 pounds
Ability to train/facilitate
Flexible work schedule with start/stop times across all shifts
Communication skills, both written and oral
Work Experience Requirements
Number of Overall Years Necessary: 0-5 years
Experience in Quality Engineering or equivalent industry disciplines preferred
Experience in medical device manufacturing regarding Quality System requirements per 21 CFR 820 and/or ISO 13485 preferred
Education Requirements
Bachelor’s Degree in Science (Engineering, Math, Natural Sciences, or related study preferred)
Specialized Skills/Technical Knowledge
Knowledge and application of basic statistics and experimental design preferred
Knowledge and experience in statistical software packages preferred (ex. Minitab)
Technical writing skill preferred.
Experience working with self-directed work teams preferred
Experience performing internal/external audits and evaluations preferred
Experience with product design and product design related regulatory requirements preferred
Knowledge and implementation of medical device Quality System requirements (FDA and ISO) preferred
ASQ Certified Quality Engineer preferred
Knowledge of Lean and Six Sigma Black Belt principles preferred
Basic technical writing skills required, advanced technical writing skills preferred
Knowledge of SAP/ERP Systems a plus
Knowledge of Microsoft Office Products (Word, Excel, Project, Access, PowerPoint)
Local Specifications (English and Local Language) About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.
EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job Segment:
Facilities, Technical Writer, Testing, Compliance, ERP, Operations, Technology, Legal
#J-18808-Ljbffr