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Quality Manager (Pharma)

Melaka Permanent MYR10,000 - MYR12,000 per month (MYR120,000 - MYR144,000 per year) View Job Description
This role will lead and establish Quality Assurance and Quality Control functions for a newly acquired manufacturing plant in Melaka, ensuring full compliance with pharmaceutical standards and GMP. This role will build the quality foundation and supporting business expansion into pharmaceutical packaging products.
  • Pioneer quality setup in a newly acquired plant
  • Working closely with decision makers with strong growth visibility

About Our Client

Our client is a growing manufacturing organisation expanding into pharmaceutical-related products through a newly acquired facility in Malaysia. The business is investing in capability building and quality excellence to support its entry into regulated healthcare and packaging segments.

Job Description

  • Develop, implement, and maintain Quality Management Systems (QMS) aligned with GMP, regulatory, and industry standards.
  • Lead all QA and QC functions, including product release, deviation management, CAPA, and document control.
  • Ensure full compliance with pharmaceutical regulations and maintain constant audit readiness for internal, external, and customer audits.
  • Oversee validation activities, including process validation, cleaning validation, and equipment qualification.
  • Manage supplier quality lifecycle, including qualification, performance monitoring, and audit execution.
  • Drive continuous improvement initiatives using quality metrics and data analysis across manufacturing processes.
  • Lead quality control operations and ensure strict adherence to established protocols within the facility.
  • Collaborate with cross-functional teams to investigate quality issues and implement effective corrective actions.
  • Prepare and present quality performance reports to senior leadership, highlighting KPIs and improvement strategies.
  • Act as the site Quality Lead, mentoring staff and supporting team growth, including hiring and developing junior quality personnel.

The Successful Applicant

  • Bachelor's degree in Engineering, Pharmaceutical Science, Chemistry, or a related field.
  • 8-12 years of quality experience within pharmaceutical manufacturing environments.
  • Strong expertise in GMP, regulatory compliance, and audit management (internal and external).
  • In-depth knowledge of Quality Management Systems and manufacturing standards.
  • Proven leadership experience in managing QA/QC teams and driving quality excellence.
  • Strong analytical and problem-solving skills to identify root causes and implement effective solutions.
  • Experience in plastic manufacturing or pharmaceutical packaging is highly preferred.
  • Demonstrated ability to work independently, build quality systems from scratch, and manage stakeholders at regional or global levels.

What's on Offer

  • Competitive annual salary and benefits package.
  • Opportunities for professional growth within the organization.
Contact
Daryl Lim
Quote job ref
JN-062026-7046513
Phone number
+603 2302 4065

Job summary

Function
Engineering & Manufacturing
Specialisation
Quality, Technical
What is your area of specialisation?
Industrial / Manufacturing
Location
Melaka
Contract Type
Permanent
Consultant name
Daryl Lim
Consultant contact
+603 2302 4065
Job Reference
JN-062026-7046513

Diversity & Inclusion at Michael Page

We don't just accept difference - we celebrate it. We encourage applicants from all backgrounds to apply for this role and are committed to building inclusive, diverse workplaces where everyone can thrive. If you require any support or reasonable adjustments during the recruitment process, please let us know.