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Sr. Quality Engineer (Medical device)
Diverse Lynx Irvine, CA
Apply
$103k-122k (estimate)
Full Time 1 Week Ago
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Diverse Lynx is Hiring a Sr. Quality Engineer (Medical device) Near Irvine, CA

Sr. Quality Engineer
Irvine CA 92618
Contract (C2C)
Experience - 5 years
Mandatory skills:: Quality Management, Medical Device, Regulatory Standards, Quality Compliance, CAPA / NC
Experience Required:-
A minimum with 5 years of related experience Quality Management in Medical Device Industry
Technical/Functional Skills
  • Knowledge of Medical procedure and corresponding Medical Equipment
  • Knowledge of Medical Equipment manufacturing processes
  • Knowledge on Quality Management and its tools & techniques
  • Knowledge about FDA, ISO 13485, ISO 14971 and compliance regulations
  • Knowledge on Medical Device Regulatory Standards, MDD and MDR
  • Knowledge on NC, CAPA, Audit processes
  • Knowledge in Statistic, Risk Management and Design control
  • Must possess good communication skills (verbal and written), familiar with project management methodology, problem solving, and presentation skills
Roles & Responsibilities
Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Pharmaceutical, procedures and guidelines, the duties and responsibilities for this position are:
•Working with other functional groups, including R&D and Operations in support of new product development, engineering projects, quality assurance activities, and lifecycle management.
•Utilizing Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
•Oversight, from a Quality NPD perspective, of the Non-Conformance Report (Client) process for BWI facilities located in the U.S.
•Develop and establish effective quality control and support associated risk management plans, AFMEA, DFMEA and PFMEA.
•Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders.
•Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, Statistical Process Control (SPC), Design of Experiments (DOE), etc.). Performs statistical analysis of data generated including but not limited to: Gauge R&R, ANOVA, Sample Size determination and variable/attribute data analysis against predetermined acceptance criteria.
•Ensure that development activities follow design control requirements (Design Trace Matrix), product is tested per applicable standards, GSPR are met per the MDR, and product is properly transferred to manufacturing per applicable specifications.
•Technical problem solving, failure analysis, and root cause determination.
•Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work.
•Recommend issue resolution to management for significant capability and compliance issues.
•Works closely with functional leadership in planning and executing project milestones.
•Plans, develops, coordinates, and directs one or more large important engineering projects or a number of small projects with many complex features.
•Carries out complex or Client assignments requiring the development of new or improved techniques or procedures.
•ssesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment, when necessary, data are insufficient or confirmation by testing is advisable.
•Responsible for communicating business related issues or opportunities to next management levels.
•Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
•Performs other duties assigned as needed.
Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.

Job Summary

JOB TYPE

Full Time

SALARY

$103k-122k (estimate)

POST DATE

05/05/2024

EXPIRATION DATE

05/20/2024

WEBSITE

diverselynx.com

HEADQUARTERS

PRINCETON, NJ

SIZE

200 - 500

FOUNDED

2002

TYPE

Private

CEO

SHUBHENDRA VARMA

REVENUE

$50M - $200M

INDUSTRY

IT Outsourcing & Consulting

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About Diverse Lynx

Diverse Lynx is a provider of mobile application development, web designing, consulting and quality assurance services.

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The following is the career advancement route for Sr. Quality Engineer (Medical device) positions, which can be used as a reference in future career path planning. As a Sr. Quality Engineer (Medical device), it can be promoted into senior positions as a Quality Assurance Engineering Supervisor that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Sr. Quality Engineer (Medical device). You can explore the career advancement for a Sr. Quality Engineer (Medical device) below and select your interested title to get hiring information.

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