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Quality Engineer

  • ... Posted on: Nov 26, 2024
  • ... Intellectt INC
  • ... Ponce, Puerto Rico
  • ... Salary: Not Available
  • ... Full-time

Quality Engineer   

Job Title :

Quality Engineer

Job Type :

Full-time

Job Location :

Ponce Puerto Rico United States

Remote :

No

Jobcon Logo Job Description :

Please find the job details and description below and if interested You can reach me at or call me at +1(732)-813-9025.

Role: Quality Engineer
Location: Ponce , Puerto Rico
Description:
  • Contribute to continuous improvements in overall product cost and quality.
  • Participate in DFM / DFA activities assuring that packaging/production processes and equipment are taken into consideration.
  • Collaborate with Quality Engineering to provide manufacturing support.
  • Create standardized work and process maps that result in an optimized production system and extended value stream.
  • Support line validation / qualification activities for including IQ, OQ , MSA and PQ.
  • Perform root Cause Analysis (RCA), NCR and CAPA responses.
  • Need to conduct qualification, verification, and validation activities to produce medical devices.
  • Work with CFT teams in troubleshooting problems on the production floor.
  • Design, develop, testing, and validate equipment and processes; analyze and interpret process models and recommend process improvements.
  • Drive the execution of various validation and PFMEA activities as per the project plan
  • Application of statistical and analytical methods such as SPC, SQC and DOE.
  • Contributor to the Capital Expense Request (CER) process, specify cost for Packaging/Labeling/ sealing equipment with consideration to product standard cost targets and capacity demands.
  • Provide detailed engineering analysis and documentation in the management of material disposition, process updates, NCR's and CAPA.
  • Execute Site acceptance test and Factory acceptance test based on North Haven
  • Execute Validation Gap analysis of various product families
  • Plan and initiate CDPs associated with the various validation activities
  • Co-ordination with stakeholders
Qualification:
  • BS Degree in Mechanical Engineering or Equivalent/MS Engineering
  • Min 3 yrs. Applicable Experience in packaging engineering, medical devices, pharmaceutical or related industry preferred. Broad knowledge of Mechanical/Manufacturing Engineering.

Jobcon Logo Position Details

Posted:

Nov 26, 2024

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-af8aab8bb414de93f1962da53fe986f8ee8cce2351c8a884d7f2c9c3411a3d35

City:

Ponce

Job Origin:

CIEPAL_ORGANIC_FEED

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Please find the job details and description below and if interested You can reach me at or call me at +1(732)-813-9025.

Role: Quality Engineer
Location: Ponce , Puerto Rico
Description:
  • Contribute to continuous improvements in overall product cost and quality.
  • Participate in DFM / DFA activities assuring that packaging/production processes and equipment are taken into consideration.
  • Collaborate with Quality Engineering to provide manufacturing support.
  • Create standardized work and process maps that result in an optimized production system and extended value stream.
  • Support line validation / qualification activities for including IQ, OQ , MSA and PQ.
  • Perform root Cause Analysis (RCA), NCR and CAPA responses.
  • Need to conduct qualification, verification, and validation activities to produce medical devices.
  • Work with CFT teams in troubleshooting problems on the production floor.
  • Design, develop, testing, and validate equipment and processes; analyze and interpret process models and recommend process improvements.
  • Drive the execution of various validation and PFMEA activities as per the project plan
  • Application of statistical and analytical methods such as SPC, SQC and DOE.
  • Contributor to the Capital Expense Request (CER) process, specify cost for Packaging/Labeling/ sealing equipment with consideration to product standard cost targets and capacity demands.
  • Provide detailed engineering analysis and documentation in the management of material disposition, process updates, NCR's and CAPA.
  • Execute Site acceptance test and Factory acceptance test based on North Haven
  • Execute Validation Gap analysis of various product families
  • Plan and initiate CDPs associated with the various validation activities
  • Co-ordination with stakeholders
Qualification:
  • BS Degree in Mechanical Engineering or Equivalent/MS Engineering
  • Min 3 yrs. Applicable Experience in packaging engineering, medical devices, pharmaceutical or related industry preferred. Broad knowledge of Mechanical/Manufacturing Engineering.

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