| Looking On-site || Test Method Validation (TMV) || Medical Device Industry || Minneapolis, MN (Onsite) at Minneapolis, Minnesota, USA |
| Email: [email protected] |
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From: Gaurav kumar, Quantum World Technologies Inc. [email protected] Reply to: [email protected] Greeting, I hope all is well with you For the following, Quantum World IT is seeking the best consultant profile. Please respond with your most recent resume if you are considering new opportunities. Looking On-site || Test Method Validation (TMV) || Medical Device Industry || Minneapolis, MN (Onsite) Must Have Technical/Functional Skills- experience Required Knowledge of Medical procedure and corresponding Medical Equipment Good experience in CAPA execution, CAPA write up Good experience in Test Method Validation (TMV) Good experience in Process Validation. 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 NC, 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 A minimum with 5+ years of related experience Quality Management in Medical Device Industry. Roles & Responsibilities Under limited supervision and in accordance with all applicable federal, state and Experience Required A minimum with 5+ years of related experience Quality Management in Medical Device Industry. Roles & Responsibilities Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, 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. Non-Conformance Report (NCR) process for Sterilmed business unit. 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, engineering change orders. Use statistical tools to analyze data, make acceptance decisions, and improve process capability, Design Controls, Design of Experiments Technical problem solving, failure analysis, and root cause determination. Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. Generic Managerial Skills Strong communication skills. Candidates must be highly proficient in reading, writing, and speaking English language. Please enter the following information is needed for submission and share your visa and Photo id Position Applied for Candidate Full Name [As per Passport] Contact Number Primary & Secondary Email ID Current Location Passport No. Work Authorization Had ever worked with TCS in Past (Required filed) Are you comfortable for on-site Had you gotten covid vaccination doses Rate expectation Gauarv Kumar Phone: +1 805 749 5070 Email: [email protected] Quantum World Technologies Inc. 4281 Katella Ave, Suite #102 Los Alamitos CA 90720 USA Keywords: rlang information technology California Idaho Minnesota North Carolina Looking On-site || Test Method Validation (TMV) || Medical Device Industry || Minneapolis, MN (Onsite) [email protected] |
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| 04:55 AM 11-Jul-24 |