Senior Quality Engineer, Operations
New Today
Why Orthofix?
Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the partner in Med Tech.
Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.
How you'll make a difference?
The Senior Quality Engineer – Operations will engage with cross functional members to drive Quality performance and to ensure that product quality meets all internal and external requirements. They will lead initiatives to improve quality and customer satisfaction. This individual will also ensure compliance with Quality system and other standards and regulations, company quality requirements and corporate objectives.
What will your duties and responsibilities be?
Assists with complaint handling investigation as assigned
Initiates Corrective Action Requests (CAPA) based on internal NCMR investigation findings as required by QMS
Tracks, trends, and reports quality metrics. Investigate and disposition non-conformances
Works with suppliers to solve problems until resolution
Works to improve quality, reduce product/process issues, cost, and lead time
Supports continuous improvement initiatives
Develops inspection procedures and test methods
Creates work instructions, procedures, protocols etc. as needed for projects
Approves QMS documentation including validations, preventive maintenance, inspection methods and other deliverables as required by the QMS
Initiates Quality Holds when needed and monitor until closure
Performs Quality Audits as assigned
Supports external audit activities from FDA, Regulatory agencies etc.
What skills and experience will you need?
Education/Certifications:
Engineering degree or equivalent
Experience, Skills, Knowledge, and/or Abilities:
6-10 years of experience working in a regulated manufacturing environment
Excellent communication skills both written and oral
Excellent analytical skills
Travel required up to 10%, therefore must be able to utilize airplane, taxi and car
What qualifications are preferred?
Education/Certifications:
N/A
Additional Experience, Skills, Knowledge, and/or Abilities:
Knowledge of Oracle, Business Objects and Excel
Experience working in Medical Device Industry
ASQ Certification
PHYSICAL REQUIREMENTS / ADVERSE WORKING CONDITIONS
No additional physical requirements or essential functions for this position
DISCLAIMER
- Location:
- Lewisville