Job Title: Quality Assurance Engineer: IV

Duration: 4 Months

Location: San Jose (SJC), CA

Description:

POSITION SUMMARY

Ensures, through global and local Product Development Process procedures and efforts, that product software are developed, tested and transferred according to established procedures that will assure that they meet all quality requirements.

Responsible to assist in the maintenance of effective Quality Systems in accordance with FDA Quality Systems Regulation, ISO 9001, ISO 13485 and other applicable country specific regulations. Participates and provides guidance to quality improvement teams on tools, techniques and management systems for quality assurance, compliance, and continuous quality improvement.

PRIMARY DUTIES

1. Quality Engineering Support for product software Design Control Process –Implement/facilitate product risk management planning as needed. Facilitate and participate in design reviews, develop quality engineering deliverables and assure Design History File (DHF) is updated as necessary.
2. Contribute in the documentation of quality systems and programs in the areas of training, change management, validation, design controls, including product verification and validation, CAPA for relevant design issues, documentation control considerations, etc. to ensure compliance with FDA and regulatory requirements.
3. Serve as contact for assigned program(s) and provide coaching / mentoring to project managers and/or product development team in regard to the product development process, design control (e.g. risk assessment), etc.
4. Review and provide feedback on product documentation to support the product development process.
5. Participate in technical or specialty design review(s) for product development or participate as QA representative in the change management process for product development.
6. Assists in the development and execution of training programs (e.g. change control, risk analysis, Design Controls, etc.).
7. Prepare for and and support regulatory and agency inspections/audits (ISO/MDSAP/etc.), investigations, and inquiries regarding the control and assessment of product design quality. Support corporate/internal design control audits.
8. Participates in CAPA activities, including investigation, effectiveness, and root cause analysis. Support implementation of corrective actions and preventive measures.
9. Function as QA subject matter expert for cross-functional development team related practices: facilitate risk management activities, provide guidance for strategy and content of requirements and specifications. Provide strategies and approvals for verification methodologies, configuration management, validation and regression testing approaches.

KNOWLEDGE, EXPERIENCE & SKILLS
Bachelor’s Degree

Will work experience be accepted in lieu of a degree? 1 Yes 0 No

If yes, number of years experience accepted in lieu of degree and type:
10+ years directly employed in R&D Quality Assurance of Medical Devices.
1. Requires a minimum of ten years experience in a related industry regulated by FDA and/or ISO.
2. Requires demonstrated competence in software development processes, and the selection and use of Quality Engineering tools, techniques, and processes.
3. Must have exposure to and knowledge of the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, IVDR, MDSAP, etc.).
4. Requires effective written and oral communication skills to interact across all levels of the organization.
5. Must have experience in and knowledge of Microsoft Office Package (Word, Excel, etc.).
6. One or more of the following certifications is desired for this role: Certified Quality Engineering (CQE), Certified Quality Auditor (CQA), Certified Software Quality Engineer (CSQE), Certified Reliability Engineering (CRE), Certified Biomedical Auditor (BCA), or Six Sigma Black Belt.

IMPACT / MANAGEMENT SCOPE

Decision making or problem solving authority: Basic

Describe empowerment, decision making, and problem solving authority.

This position is responsible to assist in the development of quality programs to facilitate continual improvement actions. Also responsible for assuring product quality and reliability during all phases of product life cycle.
Check appropriate decision making authority below:

Decisions with long term impact Decisions with short term impact
With little to no supervisory review 1

WORKING CONDITIONS
Domestic travel require 5 % of time 1 International travel required ? 5 % of time
Typical office setting 0
Home-based

Manufacturing/Operations Center 0
Laboratory with exposure to chemicals
Physical Requirements – Enter % of time for each applicable category:
Activity Not Applicable 5-10 lbs 10-25 lbs 25-50 lbs 50-100 lbs 100-150 lbs 150+ lbs

Physical Requirements – Enter % of time for each applicable job activity:
Activity Percent of Time (if applicable)
Other:
Bending
Lifting
Pushing
Pulling

Excellent personal hygiene required in production and laboratory areas.
Walking 25%
Standing 25%
Sitting 50%
Typing 40%

 

 


At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $84.00/hr.