QC Equipment Validation & System Support Specialist

Manpower Staffing Services (Singapore) Pte Ltd

Singapore

Vor Ort

SGD 66.000 - 79.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Completion bonus 1 month

Zusammenfassung

Manpower Staffing Services (Singapore) Pte Ltd is seeking a QC Associate - System Support (Equipment Qualification/ Validation/ Pharma) in Singapore. The role focuses on maintaining GMP-compliant QC lab equipment and supporting qualification activities within the QC lab.

The ideal candidate has 5+ years in pharmaceutical QC, strong GMP knowledge, and experience with equipment qualification and data integrity.

Qualifikationen

  • 5+ years of experience in quality control within the pharmaceutical industry.
  • Good knowledge of GMP and regulatory requirements.
  • Hands-on exposure to QC laboratory instruments and ALCM management.

Aufgaben

  • Update the site validation master plan and procedures related to ALCM and CPV of GXP lab equipment.
  • Support periodic analytical method control trend review and data evaluation on method performance.
  • Support life cycle management of QC lab equipment and qualification/maintenance documentation.
  • Decommission QC equipment and maintain up-to-date lab equipment inventory.
  • Participate in documentation reviews for qualifications, risk assessments, protocols, reports and deviations.

Kenntnisse

Quality control experience
GMP knowledge
Regulatory compliance
QC laboratory instruments
ALCM management

Ausbildung

Bachelor's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology

Jobbeschreibung

Manpower Staffing Services (Singapore) Pte Ltd is seeking a QC Associate - System Support (Equipment Qualification/ Validation/ Pharma) in Singapore. The role focuses on maintaining GMP-compliant QC lab equipment and supporting qualification activities within the QC lab.

The ideal candidate has 5+ years in pharmaceutical QC, strong GMP knowledge, and experience with equipment qualification and data integrity.

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