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Kerja Sepenuh Masa, Quality System Engineer di Tecomet Pulau Pinang - Maukerja

Quality System Engineer

Tecomet

Kongsi
Simpan

Lokasi Kerja

  • Bayan Lepas Pulau Pinang Malaysia

Penerangan Kerja

Tanggungjawab

Position Summary

The Quality Systems Engineer I supports the administration, monitoring, and continuous improvement of the global QS program across all sites. This role ensures compliance with applicable standards, regulatory requirements, and internal procedures.

Principle Responsibilities

  • Assist in maintaining and improving the QMS.
  • Support compliance with FDA, ISO 9001, 13485, AS9100 and other applicable standards/regulations.
  • Participate in document control activities and change control processes.
  • Support all types of audits (external and internal).
  • Support all phases of Corrective Action and/or Preventive Action (CAPA).
  • Track and report on CAPA status.
  • Assist, Support and Maintain risk management documentation.
  • Support employee training compliance.
  • Collect and analyze quality metrics (KPIs).
  • Prepare reports on Audit results, CAPA trends, Customer complaints, Process performance.
  • Support continuous improvement initiatives.
  • Collaborate with Complaint Handling, Nonconformance, Audit, and Risk Management teams to ensure proper escalation and systemic issue evaluation.
  • Support (as needed) in internal external audits.
  • Contribute to harmonization and continuous improvement of global CAPA procedures and workflows.
  • Support quality-related projects by working with manufacturing, engineering, regulatory, and operations teams.

Qualification Requirements

Credentials/Experience:

  • ASQ Certified Quality Improvement Associate (CQIA)
  • Six Sigma Yellow or Green Belt

Experience/Educational/Training Preferred:

  • Bachelor's degree in Engineering, Quality, Life Sciences, Data Analytics, or related technical discipline required.
  • Minimum of 1 years of experience in a regulated manufacturing environment (medical device preferred).
  • Exposure to Quality Management Systems (QMS) and CAPA processes preferred.
  • Basic understanding of FDA QSR (21 CFR Part 820), ISO 13485, or other regulated standards preferred.
  • Experience working with data analysis and reporting tools such as Power BI (preferred), Tableau, or similar business intelligence platforms.
  • Internship or project experience in quality analytics or process improvement is a plus.

Knowledge, Skills, and Abilities:

LANGUAGE SKILLS

  • Ability to speak, read and write in English language and Bahasa Malaysia.
  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
  • Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.

MATHEMATICAL SKILLS

  • Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry.
  • Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
  • Working knowledge of SPC and Process Validations.

Technical Skills

  • Basic knowledge of root cause analysis methodologies.
  • Proficiency in Microsoft Excel (pivot tables, data analysis functions).
  • Experience developing dashboards or visual reports using Power BI or similar tools preferred.
  • Understanding of statistical concepts such as trend analysis, control charts, and basic risk prioritization.
  • Strong data organization and reporting capability.

Peringatan Penting

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