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Manufacturing Engineer

  • ... Posted on: Feb 11, 2025
  • ... Intellectt INC
  • ... Mahwah, New Jersey
  • ... Salary: Not Available
  • ... Full-time

Manufacturing Engineer   

Job Title :

Manufacturing Engineer

Job Type :

Full-time

Job Location :

Mahwah New Jersey United States

Remote :

No

Jobcon Logo Job Description :



This is Rohith from Intellectt INC; we've got an important role Manufacturing Engineer Mahwah, NJ (Onsite) with one of our prestigious clients. Interested candidates can please send your updated resume at

Job Title - Manufacturing Engineer
Location - Mahwah, NJ (Onsite)

Responsibilities:

  • Sound Knowledge in Manufacturing Processes Orthopaedic Medical devices.
  • Good understanding of ISO 13485, GDP, GMP, change control, medical device regulations and requirements
  • Basic understanding of process engineering, documentation.
  • Strong experience in Write, Execute, Reporting of IQ,OQ, PQ protocols.
  • Working experience in conducting Process Audits with the Procedures and Identify Gaps
  • Skill in coordinating with the customer and Offshore team for work instruction creation activities and Quality control initiatives.
  • Perform quality check on the deliverables from offshore and ensure quality output.
  • Co ordinate with onsite, Offshore team and client stakeholders for project success.
  • Capacity to work at Onsite (no remote possibilities)

Jobcon Logo Position Details

Posted:

Feb 11, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-0102433fc6bc98cbe68f293c12ad91a2acaee7d2dfe0e34ec0d2ce8a57934c57

City:

Mahwah

Job Origin:

CIEPAL_ORGANIC_FEED

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This is Rohith from Intellectt INC; we've got an important role Manufacturing Engineer Mahwah, NJ (Onsite) with one of our prestigious clients. Interested candidates can please send your updated resume at

Job Title - Manufacturing Engineer
Location - Mahwah, NJ (Onsite)

Responsibilities:

  • Sound Knowledge in Manufacturing Processes Orthopaedic Medical devices.
  • Good understanding of ISO 13485, GDP, GMP, change control, medical device regulations and requirements
  • Basic understanding of process engineering, documentation.
  • Strong experience in Write, Execute, Reporting of IQ,OQ, PQ protocols.
  • Working experience in conducting Process Audits with the Procedures and Identify Gaps
  • Skill in coordinating with the customer and Offshore team for work instruction creation activities and Quality control initiatives.
  • Perform quality check on the deliverables from offshore and ensure quality output.
  • Co ordinate with onsite, Offshore team and client stakeholders for project success.
  • Capacity to work at Onsite (no remote possibilities)

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