Quality Engineer - Medical Devices QMS Knowledge of Regulatory standards CFR820 , ISO 13485 & 14971, 60601 Hands on experience on Risk Management. Good understanding of Post Market Survey and complaint handling. Design plan Medical Process DQC Deviation and CAPA preferred. Be a part of core project team and support the quality engineering across the entire development cycle • Lead product risk management, usability, reliability and design validation efforts for new product development and design change projects. • Lead the development and implementation of design verification and validation plans with project design lead. • Lead the development of Critical to Quality (CTQs), design input and output documents. • Lead the fixture qualification and test method validation. • Participate and implement tools like Design of Experiments (DOE’s), FMEA sessions, Risk Management and ensure compliance to CTQ’s and safety requirements. • Manage electronic document control and version control on all project related documents. • Ensure adherence to the quality systems and design assurance SOPs. • Lead usability, reliability, testing, verification and validation testing – internal and local vendors. • Provide statistical testing and reliability plans. • Provide quality and regulatory compliance guidance as needed to product development or design change project teams to assure country specific compliance to the laws and regulations of the targeted market for distribution. • Ensure appropriate Project/Sustaining Quality Deliverables are created and properly executed (e.g. Project Design & Development Plan, Risk Management Plan, Hazard Analysis, Use and Design FMEA, Field Assessment Plan, and Software Validation Plan if applicable). • Co-Lead CAPA efforts, and apply sound, systematic problem-solving methodologies identifying, prioritizing, communicating and driving resolution of quality issues (e.g., 5 why’s analysis, Is-Is Not analysis, and Six Sigma problem solving methodologies). • Devise and support the implementation of effective quality assurance, process controls, statistical analyses, and metrics that assure products meet or exceed quality.
Other Details
- It is a Full Time Manufacturing job for candidates with 2 - 6+ years Experience.
More about this Quality Engineer - Medical Devices job
What are the eligibility criteria for this Quality Engineer - Medical Devices job?
Ans : Candidates should have All Education levels with 2-7 years of experience for this Quality Engineer - Medical Devices job offered by Infosys in Chakan, Pune.
What salary is offered for this Quality Engineer - Medical Devices job?
Ans : Salary details will be shared during the hiring process.
What shift and timings does this job follow?
Ans : This Quality Engineer - Medical Devices job follows a Day shift.
Do you need to visit the office for this job?
Ans : Yes, candidates need to visit the office and work from the location in Chakan, Pune.
How many vacancies are there for this Quality Engineer - Medical Devices job?
Ans : There is 1 vacancy for this Quality Engineer - Medical Devices role.
Is this job open for all genders?
Ans : Yes, this Quality Engineer - Medical Devices job is open for both male and female candidates.
What is the job location for this position?
Ans : The job location for this Quality Engineer - Medical Devices position is Chakan, Pune.
What makes this Quality Engineer - Medical Devices job a good opportunity?
Ans : The employer has not disclosed the salary for this role, but it is a Full Time opportunity with 1 opening.