| Sr. Quality Engineer Process Validation at Remote, Remote, USA |
| Email: [email protected] |
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From: Anju Pathak, Tek Inspirations LLC [email protected] Reply to: [email protected] Job Description -Sr. Quality Engineer Process Validation (Accepting Onshore / Offshore candidates - for offshore need LATAM Experience.)Location: Remote Duration: 12 months Job summary/Description Seeking a highly motivated candidate with technical skills in problem-solving, critical thinking, and who is detail-oriented. Provide support to our internal Test Method Validation team under the leadership and guidance of trained team members. Work in support of Quality system improvement initiatives remediation of quality system documentation, design documentation, standard and technical Test Methods, etc. Support the TMV process for Variable and Attribute Physical test methods for products under the Feminine Care categories. The candidate will interact remotely with the research and engineering and mill laboratory locations for test execution and surrogate development as well as the execution of validation studies. Basic Qualifications Candidate must possess a bachelors degree in engineering, or a scientific or quality assurance discipline. Awareness of Design controls and change controls for FDA regulated medical devices (21 CFR 820.20 and ISO13285 standards) Awareness of Test Method Validation, Installation Qualification, and related Statistics: Study design, DOE, TM Characterization, Data Analysis (Gage R&R, Correlation, etc.), Test method validation study. Ability to create technical documentation including TMC, IQ, TMV, and Generic Verification protocols and reports. Understanding of test fixtures and test equipment such as tensile frames. Excellent written and oral communications. Ability to summarize and consolidate data and information in presentation form for cross-functional discussion. Ability to work remotely with advanced proficiency in software applications: MS Office (Outlook, Word, Excel, PowerPoint, and MS Teams). Ability to work autonomously across functional boundaries to complete projects within required timeframes while being part of a team. Preferred Qualifications: Experience in ETQ as a quality system Product Knowledge of Tampons Additional Experiences with Process Validation, Risk Management, and Quality systems. Knowledge on Test Method Development and Validation: Surrogate development and Equivalence test Please fill the required details Full Name: Current Location: Contact: Education: Email: Work Authorization: Hourly Rate: Total experience in years Awareness of Design controls and change controls for FDA regulated medical devices (21 CFR 820.20 and ISO13285 standards): Awareness of Test Method Validation, Installation Qualification, and related Statistics: Study design, DOE, TM Characterization, Data Analysis (Gage R&R, Correlation, etc.), Test method validation study: Ability to create technical documentation including TMC, IQ, TMV, and Generic Verification protocols and reports: Excellent written and oral communications. Ability to summarize and consolidate data and information in presentation form for cross-functional discussion: Preferred Qualifications: Experience in ETQ as a quality system: Product Knowledge of Tampons: Additional Experiences with Process Validation, Risk Management, and Quality systems: Knowledge on Test Method Development and Validation: Surrogate development and Equivalence test: Keywords: rlang microsoft Sr. Quality Engineer Process Validation [email protected] |
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| 08:21 PM 13-Jan-25 |