QA Site Head | API Manufacturing & GMP Quality Systems | Tuas Pharma CDMO | UP $20K #HYT

RECRUIT EXPRESS PTE LTD

Singapore

On-site

SGD 90,000 - 150,000

Full time

5 days ago
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Job summary

RECRUIT EXPRESS PTE LTD in Tuas, Singapore is seeking a dedicated Quality Assurance lead for a permanent role. The position requires API pharmaceutical manufacturing experience and at least five years in pharmaceutical quality management, with strong GMP, CAPA, deviation and audit expertise.

You will oversee the QA system, lead investigations, and manage client audits, inspections, and quality agreements. The role offers a stable career path, opportunities to mentor the QA team, and close

Qualifications

  • Degree in Pharmacy, Chemistry or related discipline.
  • API pharmaceutical manufacturing experience required.
  • Minimum 5 years of pharmaceutical quality management experience.
  • Strong GMP, CAPA, deviation, validation and audit experience.

Responsibilities

  • Lead overall site Quality Assurance and GMP compliance.
  • Establish and maintain the site Quality Management System.
  • Lead deviations, CAPA, investigations and quality reviews.
  • Manage client audits, inspections and quality agreements.
  • Review validation and quality documentation.
  • Lead and develop the site QA team.

Skills

Quality Assurance
GMP experience
CAPA
Audits

Education

Degree in Pharmacy or Chemistry

Job description

Employment Type: Permanent
Salary: Open
Location: Tuas
Transport: Islandwide Company Bus

Job Scope:

  • Lead overall site Quality Assurance and GMP compliance
  • Establish and maintain the site Quality Management System
  • Lead deviations, CAPA, investigations and quality reviews
  • Manage client audits, inspections and quality agreements
  • Review validation and quality documentation
  • Lead and develop the site QA team

Requirements:

  • Degree in Pharmacy, Chemistry or related discipline
  • API pharmaceutical manufacturing experience required
  • Minimum 5 years of pharmaceutical quality management experience
  • Strong GMP, CAPA, deviation, validation and audit experience
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