GMP QC Compliance: Method Validation & Material Release

COALESCE MANAGEMENT CONSULTING PTE. LIMITED

Singapore

On-site

SGD 60,000 - 90,000

Full time

7 days ago
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Job summary

COALESCE MANAGEMENT CONSULTING PTE. LIMITED is seeking a QC compliance professional for GMP-regulated environments in Singapore. You will support incoming material release, method validation, and equipment qualification to ensure lab processes and records meet regulatory standards.

The role requires hands-on experience with GMP documentation, data review, and cross-functional collaboration with QA, warehouse, and lab teams to maintain inspection readiness.

Qualifications

  • Experience in incoming raw-material release in GMP/pharma environments.
  • Knowledge of the analytical method validation lifecycle.
  • Experience validating raw-material analytical methods.
  • Exposure to laboratory equipment qualification.
  • Strong GMP documentation practices and quality-system awareness.

Responsibilities

  • Support and coordinate incoming material release activities.
  • Manage or contribute to analytical method validation lifecycle.
  • Apply method-validation principles to raw-material testing methods.
  • Support equipment qualification activities for laboratory equipment.
  • Prepare, review, and maintain GMP-compliant QC documentation.
  • Work with QC, QA, warehouse and other stakeholders to resolve issues.
  • Maintain inspection readiness and follow site quality procedures.

Skills

Raw-material release
Analytical method validation
Laboratory equipment qualification
GMP documentation
Cross-functional collaboration

Education

Bachelor's degree in Chemistry/Pharmaceutical Sciences

Job description

COALESCE MANAGEMENT CONSULTING PTE. LIMITED is seeking a QC compliance professional for GMP-regulated environments in Singapore. You will support incoming material release, method validation, and equipment qualification to ensure lab processes and records meet regulatory standards.

The role requires hands-on experience with GMP documentation, data review, and cross-functional collaboration with QA, warehouse, and lab teams to maintain inspection readiness.

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