Quality Assurance Specialist (IATF16949/ISO9001)

at  MANFIELD EMPLOYMENT SERVICES PTE LTD

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate28 Sep, 2024USD 6000 Monthly28 Jun, 2024N/AGood communication skillsNoNo
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Description:

  • Managing QMS improvement initiative across all departments and functions to ensure quality initiatives and quality plans are executed and maintained in full compliance with IATF requirements.
  • Review batch release activities for production including but not limited to review of product grading records, analytical data, Certificate of Analysis (COA) and other documents as needed for consistency with applicable regulations and for compliance with Company Quality System. Approve these records when Assistant / QA or Quality Manager delegates accordingly.
  • Release, review and verify CAPA quality related issues (Raw Material, Finished Product, Shipment & Logistics issues) and ensure effectives of corrective actions. ETQ Administrator for CAPA and Document Control.
  • Generate and review IATF / ISO procedures and Quality related procedures / instructions.
  • Drive CPK improvement, review control charts, MSA and GR&R and recommend improvement action.
  • Drive FMEA and Control Plan generation and revision.
  • Manage IATF Core Tools (PPAP, APQP) documentation and reports.
  • Assist Assistant / QA or Quality Manager during plant audits (customer audit, external, internal and Supplier audit). Follow up completion of plant audit findings corrective / preventive actions
  • Lead Auditor for IATF / ISO Internal Audit and report nonconformity and recommends opportunities for improvement.
  • Support Assistant / QA or Quality Manager in handling customer complaint & investigation.
  • To make judgments in solving variances and help production in resolving issues related to quality
  • Participate in Plant 5S / Housekeeping Initiatives and Safety Committee Meeting.
  • Participate in Production Meeting, Annual IATF / ISO Management Review, Quality Committee Meeting (QCM) and Production Quality Meeting (PQM).

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Software Testing, Clinical Pharmacy

Graduate

Proficient

1

Singapore, Singapore