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QC Specialist – Analytical Methods, GxP Lab Equipment & LIMS (Pharma) - Islandwide, SG

QC Specialist – Analytical Methods, GxP Lab Equipment & LIMS (Pharma) - Islandwide, SG

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTDIslandwide, SG
11 days ago
Job description

Roles & Responsibilities

QC Specialist – Analytical Methods, GxP Lab Equipment & LIMS (Pharma)

Salary Up to $7,000 depending on experience

Location : Tuas

Industry : Pharmaceutical

Our client is a global leader in the pharmaceutical industry, producing and delivering over 4 billion units of medicines and vaccines each year—making a real difference in getting life-saving treatments to those who need them most. They are driving the future of healthcare with state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation, ensuring medicines reach patients faster, safer, and more sustainably.

Responsibilities :

  • Represent the site in global Communities of Practice (CoPs) and Centers of Excellence (CoEs) for QC processes and ensure effective local communication.
  • Maintain the site Validation Master Plan and procedures related to Analytical Lifecycle Management (ALCM) and Continued Process Verification (CPV) for GxP laboratory equipment.
  • Oversee lifecycle management, qualification, and maintenance of QC lab equipment, ensuring compliance with regulatory and quality standards.
  • Lead and support analytical method lifecycle activities including method reviews, trending, data evaluation, and compendial compliance.
  • Drive implementation and maintenance of QC digital solutions (e.g., LIMS), including data integrity and end-user management.
  • Support and investigate quality control events, deviations, and CAPAs within the QC scope.
  • Coordinate documentation, review, and approval of qualification deliverables (e.g., risk assessments, protocols, reports).
  • Provide technical leadership in analytical validation, method transfers, and lab projects.
  • Act as SME for laboratory computerized systems and provide system administrator support.
  • Support regulatory inspections and customer audits by presenting relevant documentation and records.
  • Ensure safe laboratory operations and compliance with HSE and cGMP requirements.
  • Deputize for QC Manager as required.

Requirements

  • Ideally 5 years of experience in quality control within pharmaceutical with knowledge of Good Manufacturing Practices (GMP), regulatory requirements and expertise on lab instruments.
  • Excellent interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.
  • Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements.
  • Knowledge of the quality systems and associated technologies.
  • Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement.
  • Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
  • Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
  • Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
  • Experienced in analytical method continuous monitoring requirements.
  • Lim Pey Chyi - Apple.lim@manpower.com.sg

    Recruitment Consultant (R2090579)

    Manpower Staffing Services (S) Pte Ltd

    EA Licence : 02C3423

    Tell employers what skills you have

    GxP

    Pharmaceutical Industry

    Producing

    Quality Control

    Staffing Services

    Healthcare

    Compliance

    Attention to Detail

    LIMS

    Audits

    Regulatory Requirements

    Technical Leadership

    Laboratory

    Manufacturing

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    Qc Specialist • Islandwide, SG

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