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Specialist QA - 34063

Juncos, Puerto Rico
Description:
  • Perform one or more of the following duties and responsibilities in support of  Company's Quality Assurance program under minimal supervision.
Functions: 
  • Review and approve product MPs.
  • Approve process validation protocols and reports for manufacturing processes. - Request Quality on incident triage team.
  • Approve Environmental Characterization reports.
  • Release of sanitary utility systems.
  • Approve planned incidents.
  • Represent QA on NPI team.
  • Lead investigations.
  • Lead site audits.
  • Own site quality program procedures.
  • Designee for QA manager on local CCRB.
  • Review Risk Assessments.
  • Support Automation activities.
  • Support facilities and environmental programs.
  • Review and approve Work Orders.
  • Review and approve EMS/BMS alarms.
  • Approve NC investigations and CAPA records.
  • Approve change controls.
  • Provide lot disposition and authorize lots for shipment.
Education:
  • Doctorate degree
  • Master's degree and 3 years of directly related experience
  • Bachelor's degree and 5 years of directly related experience
  • Associate's degree and 10 years of directly related experience
  • High school diploma / GED and 12 years of directly related experience.
Preferred Qualifications:
  • Quality Professional with Manufacturing Process Audit and Batch Record Review experience.
  • Knowledge or to be familiar with DAI process, PASx/MES application, MAXIMO, SAP and LIMS.
  • Available for non-standard shift which includes nights and weekends.
Competencies/Skills: 
  • Project management skills.
  • Strong organizational skills, including ability to follow assignments through to completion.
  • Initiate and lead cross functional teams.
  • Enhanced skills in leading, influencing and negotiating.
  • Strong knowledge in area of expertise.
  • Collaborate and coordinate with higher level outside resources.
  • Strong knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development.
  • Demonstrate ability to interact with regulatory agencies.
  • Strong word processing, presentation, database and spreadsheet application skills.
  • Strong communication (both written and oral), facilitation and presentation skills.
  • Strong skill in working independently and to effectively interact with various levels.
  • Advanced data trending and evaluation.
  • Ability to evaluate compliance issues.
  • Demonstrate the Company's Values/Leadership Practices.
Work Methodology: 
  • 100 % On-Site
  • 11 months (1st Contract)
  • 12hrs Shifts (5:00pm to 5:30am) Available for non-standard shift which includes nights and weekends.
  • Professional  Services Contract 

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