Error 2318 ::The remote server returned an error: (404) Not Found. Biology Job Mesa Arizona | Quality Assurance Investigator Pinpoint Pharma

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Biology Job in Mesa, Arizona : AZ

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Quality Assurance Investigator

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Pinpoint Pharma
QA - Quality Control, Research
Mesa
Arizona
click here to apply

Quality Assurance Investigator Job Description

The Quality Assurance Investigator will be responsible for the following:


Job Overview:
Execute Investigations, Root Cause Analysis, Correction, Corrective and Preventive Action activities in accordance with the company's Quality System.

Job Duties:

  • Execute Investigations, Root Cause Analysis, Correction, Corrective and Preventive Action activities in accordance with the company's Quality System.  
  • Facilitate weekly Material Review Board Meeting and monthly CAPA Review Board Meeting.  
  • Track, Trend and Maintain Metrics on the CAPA System.  
  • Train users on the CAPA process and QMS tools utilized in the execution of CAPAs and NCRs.  
  • Generate, review and approve internal operating procedures and specifications.  
  • Assist with continued company certification to the appropriate Quality System Standards and Regulations, and assist with all related inspections as required.



Mesa Biology Job

Quality Assurance Investigator Job Requirements

  • BS in a Physical Science or Engineering or Equivalent Experience Required
  • Minimum 2-4 years Quality Assurance and/or other regulated industry or similar experience required
  • Strong technical writing and general problem-solving skills required. 
  • Must be proficient in MS Word, Excel, and PowerPoint software programs.
  • Excellent verbal and written communication skills required.
  • Ability to work with company staff and communicate effectively throughout the organization is essential.
  • Preferred experience with statistical analysis of data. 
  • Preferred experience with the sterilization of medical devices. 
  • Preferred experience in performing internal and/or supplier audits. 
  • Preferred experience in training of personnel. 
  • Familiar with ISO 9000/ISO 13485 Quality System Standards, FDA Quality System Regulations, GMPs, and/or other international medical device regulations.
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