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Qa director

https://www.randstad.com Logo

Randstad

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Location:
Malaysia , Selangor

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Category:
Manufacturing

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Contract Type:
Not provided

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Salary:

25000.00 - 45000.00 MYR / Month
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Job Description:

We are currently looking for a QA Director for a leading player in the Chemical Manufacturing Industry for their expansion. This company has a legacy of more than 30 years in Malaysia. This position requires your urgent attention. Based in Selangor. Reporting to: COO.

Job Responsibility:

  • Lead Quality Assurance strategy across plant and central functions, ensuring alignment with business objectives and regulatory expectations
  • Define and execute long-term quality improvement roadmaps, maintaining and strengthening enterprise QMS compliance (ISO 13485, FDA QSR, MDR)
  • Standardize and govern core QA processes across all sites, including CAPA, change control, complaints, audits, validation, calibration, and laboratory operations
  • Drive QA performance management through KPIs, benchmarking, structured reviews, and sustained corrective and preventive actions
  • Direct regulatory inspection and key customer audit readiness, serving as the escalation point for critical quality issues, regulatory findings, and supplier non-conformances
  • Lead enterprise risk management and cross-functional root cause investigations to deliver robust, long-term preventive solutions for systemic quality issues
  • Oversee quality integration in NPI/NPD initiatives, QA budgeting, and resource planning to ensure effective execution and compliance
  • Develop QA leadership and talent through coaching, succession planning, and knowledge sharing, while fostering a strong quality culture and strategic partnerships with internal and external stakeholders

Requirements:

  • Bachelor’s or Master’s degree in Engineering, Science, or a related field
  • Minimum of 15 years in manufacturing, including at least 8 years in managerial roles
  • Proven leadership in Quality Management Systems (QMS), regulatory compliance, customer interactions, cross-plant QA oversight, and regulatory inspection readiness
  • Strong knowledge of GMP and manufacturing technologies
  • Expertise in QMS standards including FDA QSR (21 CFR 820), ISO 13485, and ISO 9001

Additional Information:

Job Posted:
January 09, 2026

Expiration:
February 26, 2026

Work Type:
On-site work
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