Attindas Hygiene Partners Group
Quality Assurance Engineer II
Attindas Hygiene Partners Group, Greenville, North Carolina, United States, 27834
Attindas Hygiene Partners
designs, manufactures, and markets absorbent hygiene products. The company sells adult incontinence and infant diapers, among other products, into the healthcare, retail, and direct-to-consumer channels under brands including Attends, Indas, and Comfees as well as a wide range of private label brands for retailers.
Mission We champion health, dignity and comfort.
Vision To be a global leader in absorbent hygiene by meeting consumers’ diverse needs through effective, affordable and widely available personal care solutions.
Our Values Caring, Agile, Innovative, Unique, Personal, Genuine
Job Summary The QA Engineer II is responsible for ensuring QA System compliance and capability through ownership, development, implementation, and continuous improvement of quality systems within the site. The QA Engineer II is responsible for the daily QA lab activities and staffing.
Key areas of the role Development, Implementation and Management of Quality Systems at the Site.
Owner of the site's quality systems to ensure compliance to the corporate quality system and site procedures.
Document Control Site System Owner
Internal Audit Program Owner
Mock Recall & Traceability Process Owner
Corrective & Preventative Action System Owner
QMS Training Lead for the site
Electronic QMS System Key User for the site
Others as assigned by QA manager
Provides updates and ongoing health checks of the processes.
Supports plant goals by implementing systems to support continuous improvement.
Leads/Supports All Internal and External Quality Audits
Internal Audit Owner
GMP Monthly Inspection (Coordination and Metrics)
Leads / Supports External Audits as required.
Enhancing Operations Quality Capability & Ownership through Training, Coaching and Supporting
Provides site wide quality systems training, coaching and support
Leads the transfer of identified quality systems to the QA Technicians by providing system development, training and ongoing coaching
Leads various elements of the process control strategy
Backup product release support as needed
Serves as the backup to the QA manager as needed
Continuous Improvement
Lead continuous improvement activities including transferring from a heavy product testing to online capability controls
Work across other sites to standardized best in class approaches / processes
Leads lab operations and supervises lab personnel
Perform other duties as assigned.
Required Qualifications/Professional Experiences
Bachelor’s degree in Engineering or related technical field
5-7 years of experience implementing and managing quality systems
Experience developing and implementing site quality systems compliant with corporate requirements
Work effectively with teams and individuals
Strong IT skills, including MS Word, Excel, PowerPoint, and related MS Office applications.
1-3 Years Management and/or Supervisory Experience
Preferred Qualifications/Professional Experiences/Years of Experience
Prior experience in a regulated manufacturing environment (Medical, Pharma or Food)
Advanced Microsoft office skills (excel, word)
Experience developing and implementing quality systems
Green Belt Six Sigma Training
#J-18808-Ljbffr
designs, manufactures, and markets absorbent hygiene products. The company sells adult incontinence and infant diapers, among other products, into the healthcare, retail, and direct-to-consumer channels under brands including Attends, Indas, and Comfees as well as a wide range of private label brands for retailers.
Mission We champion health, dignity and comfort.
Vision To be a global leader in absorbent hygiene by meeting consumers’ diverse needs through effective, affordable and widely available personal care solutions.
Our Values Caring, Agile, Innovative, Unique, Personal, Genuine
Job Summary The QA Engineer II is responsible for ensuring QA System compliance and capability through ownership, development, implementation, and continuous improvement of quality systems within the site. The QA Engineer II is responsible for the daily QA lab activities and staffing.
Key areas of the role Development, Implementation and Management of Quality Systems at the Site.
Owner of the site's quality systems to ensure compliance to the corporate quality system and site procedures.
Document Control Site System Owner
Internal Audit Program Owner
Mock Recall & Traceability Process Owner
Corrective & Preventative Action System Owner
QMS Training Lead for the site
Electronic QMS System Key User for the site
Others as assigned by QA manager
Provides updates and ongoing health checks of the processes.
Supports plant goals by implementing systems to support continuous improvement.
Leads/Supports All Internal and External Quality Audits
Internal Audit Owner
GMP Monthly Inspection (Coordination and Metrics)
Leads / Supports External Audits as required.
Enhancing Operations Quality Capability & Ownership through Training, Coaching and Supporting
Provides site wide quality systems training, coaching and support
Leads the transfer of identified quality systems to the QA Technicians by providing system development, training and ongoing coaching
Leads various elements of the process control strategy
Backup product release support as needed
Serves as the backup to the QA manager as needed
Continuous Improvement
Lead continuous improvement activities including transferring from a heavy product testing to online capability controls
Work across other sites to standardized best in class approaches / processes
Leads lab operations and supervises lab personnel
Perform other duties as assigned.
Required Qualifications/Professional Experiences
Bachelor’s degree in Engineering or related technical field
5-7 years of experience implementing and managing quality systems
Experience developing and implementing site quality systems compliant with corporate requirements
Work effectively with teams and individuals
Strong IT skills, including MS Word, Excel, PowerPoint, and related MS Office applications.
1-3 Years Management and/or Supervisory Experience
Preferred Qualifications/Professional Experiences/Years of Experience
Prior experience in a regulated manufacturing environment (Medical, Pharma or Food)
Advanced Microsoft office skills (excel, word)
Experience developing and implementing quality systems
Green Belt Six Sigma Training
#J-18808-Ljbffr