Bachelor's degree in Engineering, Life Sciences, or related field.
6+ years of quality engineering experience in the medical device industry or a regulated manufacturing environment.
Hands-on expertise in root cause analysis tools (5-Why, Fishbone, Lean, Six Sigma).
Practical experience with risk management tools (PFMEA).
In-depth knowledge of ISO 13485, ISO 14971, IEC 60812, and 21 CFR 820 QMSR standards.
Fluency in English.
Responsibilities
Support translation of process risk into PFMEA controls and control plans.
Ensure robust validations and verifications, overseeing revalidation cycles.
Enforce strict adherence to manufacturing-related procedures.
Collaborate with manufacturing engineering to optimize inspection and testing methods.
Participate in NPI and Lifecycle projects for compliant execution.
Document and track production non-conformances, leading root-cause analysis and CAPA actions.
Utilize data to detect variation and drive continuous improvement.
Benefits
Support for internal and external audits.
Lead supplier audits.
Opportunities for continuous improvement training.
Participation in critical and time-sensitive topics like recalls and production issues.
Full Job Description
Job Description:
JOB SUMMARY:
The Quality Assurance Engineer is responsible to ensure that production processes remain in a state of control, validation and verification activities are robust, and processes consistently produce medical devices that meet specifications. This role supports and ensures compliant execution of New Product Introduction and manufacturing Life Cycle Management activities and drive continuous improvement activities.
PRIMARY DUTIES & RESPONSIBILITIES:
Support the translation of process risk into PFMEA controls, control plans, standard work and -for-purpose in-process inspection.
Ensure validations and verifications are robust, and oversee revalidation cycles.
Ensure manufacturing-related procedures are strictly applied.
Partner with manufacturing engineering to optimize inspection and testing methods.
Participate in NPI and Lifecycle projects to ensure compliant execution thereof.
Document, evaluate and track production non-conformances, and lead or facilitate containment, root-cause analysis, NCR and CAPA actions
Use process, inspection and nonconformance data to detect variation, confirm capability and drive continuous improvement
Partner with Operations and Engineering to follow standard work, manage changes and maintain accurate, traceable records.
Support critical and time-sensitive topics, such as recalls, production issues, internal and external audits, corrective and preventive action
Support the creation, implementation, training and continuous improvement of Quality Assurance processes.
Act as a consultant for project teams and individuals related to application and interpretation of internal and external procedures, guidance, standards and regulation to find pragmatic ways to achieve appropriate and compliant documentation of activities.
General Quality Accountabilities
Support internal, and external audits
Lead supplier audits
Job Requirements:
Bachelor's degree in Engineering, Life Sciences or related disciplines.
6+ years of quality engineering experience in the medical device industry or equivalent regulated industry in a manufacturing environment.
Hands-on expertise in root cause analysis tools such as 5-Why, Fishbone, Lean or Six Sigma methodologies.
Practical experience with risk management tools (PFMEA).
In-depth understanding and knowledge on standards and regulation including but not limited to:
ISO 13485 - Medical devices - Quality management systems - Requirements for regulatory purposes.
ISO 14971 - Medical devices - Application of risk management to medical devices.
IEC 60812 - Failure modes and effects analysis (FMEA and FMECA).
21 CFR 820 QMSR - Quality Management System Regulation (FDA).
Fluency in English.
PREFERRED QUALIFICATIONS:
Master's Degree preferred.
Exercises independent work style and judgment in complex quality and compliance topics.
Applies risk-based thinking.
Effective verbal and written communication skills across functions.
Strong analytical, statistical, and documentation capabilities.
Objective problem-solving skills with the ability to make firm, risk-based quality decisions under pressure.
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Target Market Salary Range:
Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs. The disclosed reasonable estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Envista, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. The total compensation package for this position may also include an annual performance bonus, medical/dental/vision benefits, 401K match, and/or other applicable compensation plans.
For Field Sales roles, the salary range listed reflects base pay only and does not include incentive pay opportunities under the applicable sales compensation plan
$105,200 - $128,600
Operating Company: Nobel Biocare
About enVista
enVista is a global software solutions and consulting services firm headquartered in Carmel, Indiana. The company provides consulting, implementation, and managed services in supply chain, transportation, retail, and IT. enVista's services include supply chain strategy, transportation management, warehouse management, labor management, and IT services. The company has offices in North America, Europe, and Asia.