Quality Assurance Engineer-Validation
Company: Enovis
Location: Austin
Posted on: January 23, 2025
Job Description:
Job Description:At Enovis we pay attention to the details. We
embrace collaboration with our partners and patients, and take
pride in the pursuit of scientific excellence - with the goal of
transforming medical technology as we know it.Because that's how we
change the lives of patients for the better. And that's how we
create better together. Why work at Enovis? .As a key member of our
Quality team, you will play an integral part in helping Enovis
drive the medical technology industry forward through transforming
patient care and creating better patient outcomes.Job Title:Quality
Assurance Engineer - ValidationReports To:Sr. Quality Program
ManagerLocation:Austin, TXBusiness Unit Description:Surgical
Process ValidationJob Title/High Level Position Summary:Working
cross-functionally, conduct technical and complex quality analysis
and tests of quality control program and recommend necessary
quality procedure changes. Record and analyzes customer claims and
prepare reports on rejected or defective products. Assist in the
development of new methods and procedures.Essential
Responsibilities:
- Involvement in the Master Validation Plan (IQ, OQ, PQ)
regarding validation and verification Processes
- Participate in continuous improvement activities to enhance
quality systems, such as 5S, Kaizen lean methods, etc.
- Interface with Engineering and Operations to ensure transfer to
Production of new products are in accordance with approved
data.
- Support the Quality Inspectors/Techs to ensure that products
and processes comply with the relevant requirements of the quality
management system (QMS).
- Participate in audits, including Notified Body Audits, FDA
inspections and other 3rd party audits as well as closingout audit
findings, creating audit finding reports and determine proper
corrective and preventive actions.
- Analyze failure, corrective and preventive actions needed to
respond to customer complaints/supplier failures.
- Maintain company quality documentation, such as quality
manuals, quality procedures, etc.
- Maintain Nonconformance System and the COPQ Initiatives.
- Facilitate and Manage Gage R&R, SPC and capability
requirements
- Participate on launch and current production engineering
changes
- Supports Incoming Inspection; help maintain files and backup
supplies for inspection.
- Currently, Enovis does not provide sponsorship for employment
visas (e.g., H-1B) and will not offer such sponsorship in the
future. Applicants must already have full-time work authorization
in the United States, both now and in the future, without requiring
sponsorship.Minimum Basic Qualifications:To perform this job
successfully, an individual must be able to perform essential
duties satisfactorily. The requirements listed below are
representative of the knowledge, skill, and/or ability required:
- A bachelor's degree in engineering or other technical
discipline degree is required
- A minimum of 2 years of experience in quality engineering or
related field with, with focus on, process validations, product
development supports
- Previous knowledge of FDA/GMP, CMDR, MDD and ISO 13485 quality
standards.
- Experience with Quality related tools (D and P FMEA, QFD, SPC,
Risk Analysis, DOE, and TQM)
- Previous experience with Microsoft Word, or equivalent word
processing software; Excel, or equivalent spreadsheet software, as
well as statistical analysis and data base searches.Desired
Characteristics:Certifications, Skills, Competencies
- Previous working knowledge of US and International quality
system regulations.
- Proven project management skills; able to complete technical
projects with minimal supervision. Strong interpersonal
communication and teamwork skill.
- ASQ certification with active local membership is
preferred.
- Lean Six Sigma Green Belt or higher preferred.
- Ability to understand and interpret drawings and data -
GD&T knowledge to interpret mechanical part drawings, assembly
drawings, block and flow diagrams, and BOMs
- Agile and Oracle experience highly desired.
- Experience in the Medical Device Industry and lean
manufacturing is a plus.
- Must have statistical aptitude and understand concepts of
geometric dimensioning and tolerance and knowledge of problem
solving techniques.
- Personal computer skills are required, as well as excellent
verbal and written communication skills.
- Application and implementation of regulations such as
GMP/QSR/ISO/MDD and Canadian Medical Devices a plus"Creating better
together". It's the Enovis purpose, and it's what drives us and
empowers us every day on a global scale. We know that the power to
create better - for our customers, our team members, and our
shareholders - begins with having the best team, pursuing common
goals, operating at the highest levels, and delivering
extraordinary outcomes.Watch this short video and discover what
creating better together means to us at Enovis:ABOUT ENOVISEnovis
Corporation (NYSE: ENOV) is an innovation-driven medical technology
growth company dedicated to developing clinically differentiated
solutions that generate measurably better patient outcomes and
transform workflows. Powered by a culture of continuous
improvement, global talent and innovation, the Company's extensive
range of products, services and integrated technologies fuels
active lifestyles in orthopedics and beyond. Visit to learn
more.EQUAL EMPLOYMENT OPPORTUNITY: Enovis provides equal employment
opportunities based on merit, experience, and other work-related
criteria and without regard to race, color, ethnicity, religion,
national origin, sex, age, pregnancy, disability, veteran status,
or any other status protected by applicable law. We also strive to
provide reasonable accommodation to employees' beliefs and
practices that do not conflict with Enovis policies and applicable
law. We value the unique contributions that every employee brings
to their role with Enovis. ABOUT ENOVISEnovis Corporation (NYSE:
ENOV) is an innovation-driven medical technology growth company
dedicated to developing clinically differentiated solutions that
generate measurably better patient outcomes and transform
workflows. Powered by a culture of continuous improvement, global
talent and innovation, the Company's extensive range of products,
services and integrated technologies fuels active lifestyles in
orthopedics and beyond.For more information about Enovis, please
visit .EOE AA M/F/VET/Disability StatementAll qualified applicants
will receive consideration for employment and will not be
discriminated against on the basis of race, religion, color,
national origin, sex, protected veteran status, disability, or any
other basis protected by federal, state or local laws.
Keywords: Enovis, Pflugerville , Quality Assurance Engineer-Validation, Engineering , Austin, Texas
Didn't find what you're looking for? Search again!
Loading more jobs...