We have other current jobs related to this field that you can find below

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    3 months ago

    West Terre Haute, United States Marion Manufacturing Full time

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  • Mechanical Engineer III

    2 weeks ago

    West Valley City, United States bioMerieux Full time

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  • Continuous Improvement Engineer III

    3 months ago

    Kansas City, United States Milbank Manufacturing Full time

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  • Automation & Controls Engineer III

    3 months ago

    West Valley City, United States Dennis Group Full time

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  • Mechanical Engineer III

    1 month ago

    Simi Valley, United States CV Library Full time

    Overview: Must be a US Person (US Permanent or US Citizen). Hybrid opportunity with the expectation of being on site 20% of the time. Candidates should be local to southern California able to attend meetings at facility in Simi Valley with minimal notice if needed. Relocation assistance available. Full-time Direct Employment, W2 with full benefits. The US...

  • Mechanical Engineer III

    1 month ago

    Simi Valley, United States Columbus Sverige Full time

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  • Automation Engineer III

    1 month ago

    Salt Lake City, United States Astrix Technology Full time

    Automation Engineer III Manufacturing Salt Lake City, UT, US Pay Rate Low: 64.80 | Pay Rate High: 84.89 + Added - 19/07/2024 Apply for Job Our client is a global medical device company whose passion is to deliver high quality life-saving products. They are looking for an Automation Engineer III to join their team! **Pay:** $40-$46/hr **Location:**...

  • Quality Engineer

    2 days ago

    West Valley City, United States Safeguard Global Recruiting Full time

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  • Mechanical Engineer III

    1 month ago

    Simi Valley, United States Columbus Technologies Full time

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  • Operator Manufacturing III NU

    5 days ago

    West Memphis, United States Coca-Cola Consolidated Full time

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  • Engineer-RF - III

    3 weeks ago

    West Henrietta, United States Randstad North America, Inc. Full time

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  • Manufacturing Engineer

    1 week ago

    Fountain Valley, United States ISC - Interconnect Solutions Company Full time

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  • Manufacturing Engineer

    1 week ago

    Fountain Valley, United States ISC - Interconnect Solutions Company Full time

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  • Manufacturing Engineer

    2 weeks ago

    West Torrington, United States Aptyx Full time $70,000

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  • Manufacturing Engineer

    3 weeks ago

    West Lafayette, United States Forward March Inc. Full time

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  • Manufacturing Engineer

    3 months ago

    West Lafayette, United States Forward March Inc. Full time

    Job DescriptionJob DescriptionForward March Inc.,is partnering with a leading company in Aerostructures and is seeking a highly skilled and motivated Manufacturing Engineer to join our team. Forward March Inc. partners with this Aerostructures company in West Lafayette to manufacture aircraft for the United States Airforce. We are looking to fast track...

  • Manufacturing Engineer

    3 weeks ago

    West Greenwich, United States ACL Digital Full time

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  • Manufacturing Engineer

    2 weeks ago

    West Bridgewater, United States HireFocus LLC Full time

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  • Mechanical Design Engineer III-IV

    3 weeks ago

    Oklahoma City, United States Kratos Defense Full time

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  • Manufacturing Engineer

    1 month ago

    West Greenwich, United States ACL Digital Full time

    Title: Senior Engineer Location: West Greenwich, RIDuration: 12 months The Engineer role will provide direct engineering technical support as follows:• Identify, support, and/or lead implementation of engineering based improvements or upgrades to the equipment systems. This may include development of reason for improvement and identification of design...

Manufacturing Engineer III

2 months ago

West Valley City, United States Aditi Consulting Full time

Responsibilities: Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on Test Method Validation and EUMDR Validation Remediation of medical devices. Provide statistical analysis of the date to support the reports. Troubleshooting equipment/processes that do not perform as intended during validation runs. Recommend process/quality improvements as part of validation runs. Evaluate, investigate and document non-conformances incidents and/or protocol deviations. Complete assigned Non-Conformance and CAPA investigations and prepare investigation reports. Develop and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel. Work on project teams with other internal departments, external vendors, and customers as required. Assure that existing processes and assigned activities fully comply with regulatory and/or international agencies, such as FDA, ISO, OSHA, EPA, among others. Participate in the compilation and review of technical documentation for both domestic and international regulatory submissions. Participate in external audits such as: FDA, Notified Body (BSI) and Corporate, among others. Performs other related duties as necessary. Qualifications: Knowledge of FDA, OSHA, EPA, and GMP's and ISO requirements. Knowledge in Organizational Excellence and Lean/Six Sigma. Strong Project Management skills. Ability to lead teams through complex projects and provide departmental technical leadership. Must have excellent communication skills and a strong track record of working cross-functionally. Must have demonstrated ability to think strategically. Able to develop technical documentation such as: Change Controls, Validation Plans, Validation Protocols, Technical / investigation reports, SOP, and others. Teamwork oriented and self-starter. Education and/or experience: BS in Engineering, preferably Mechanical, Manufacturing, Industrial, Electrical, Chemical, or Biomedical (Professional Engineer License.) or sciences related field. Lean/Six Sigma Green or Black Belt Certification is a plus. Experience in validations such as: manufacturing equipment, manufacturing processes, Test Method validation, stability or aging, required. Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment. Responsibilities: Generate Gap Assessment for Design Files to EUMDR standard, including Validations, Labeling, Risk Files etc. Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices. Provide statistical analysis of the date to support the reports. Generation and implementation of change controls and engineering notices (ECO). Develop statistically based sampling plans for in-process and final testing and inspections, and validations. Troubleshooting equipment/processes that do not perform as intended during validation runs. Recommend process/quality improvements as part of validation runs. Evaluate, investigate and document non-conformances incidents and/or protocol deviations. Complete assigned Non-Conformance and CAPA investigations and prepare investigation reports. Develops and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel. Work on project teams with other internal departments, external vendors, and customers as required. Assure that existing processes and assigned activities fully comply with regulatory and/or international agencies, such as FDA, ISO, OSHA, EPA, among others. Participate in the compilation and review of technical documentation for both domestic and international regulatory submissions. Participate in external audits such as: FDA, Notified Body (BSI) and Corporate, among others. Performs other related duties, as necessary. Compensation: The pay rate range above is the base hourly pay range that Aditi Consulting reasonably expects to pay someone for this position (compensation may vary outside of this range depending on several factors, including but not limited to, a candidate’s qualifications, skills, competencies, competencies, competencies, competencies, experience, location and end client requirements). Benefits and Ancillaries: Medical, dental, vision, PTO benefits and ancillaries may be available for eligible Aditi Consulting employees and vary based on the plan options selected by the employee. Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions.