Pharma QA Specialist, GMP & QMS (Contract)

Manpower Staffing Services (Singapore) Pte Ltd

Singapore

On-site

SGD 25,000 - 42,000

Full time

3 days ago
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Benefits offered by this job

Training Provided

Job summary

Manpower Staffing Services (Singapore) Pte Ltd invites applications for a QA Specialist role focusing on GMP-compliant QMS, document control, training, supplier management, and CAPA. You will ensure data integrity and support continuous improvement within cGMP standards at our Jurong facility.

The contract position requires 1-3 years in pharmaceutical quality, familiarity with TrackWise or similar QMS, and strong collaboration across teams to uphold regulatory commitments and client expectations.

Qualifications

  • 1–3 years of pharmaceutical quality experience.
  • Experience with QMS; TrackWise is an asset.
  • Biologics and aseptic training is an asset.
  • Site data integrity management experience is an asset.

Responsibilities

  • Write and review SOPs and procedures.
  • Maintain QMS systems and ensure GxP compliance.
  • Oversee change control, CAPA actions, and effectiveness checks.
  • Coordinate document management and archiving.
  • Support supplier management and Quality Agreements.
  • Lead site self-inspection programs and audits readiness.
  • Aggregate and analyze quality data for management reviews.
  • Provide training on GMP and quality systems.
  • Maintain data integrity system and ensure timely CAPA closures.
  • Support regulatory and client audits.

Skills

QMS oversight
GxP compliance
CAPA management
Document control
Data integrity
Quality improvement
Audit readiness
Cross-functional collaboration
Quality risk management

Education

Bachelor’s Degree in Life Sciences or related field

Tools

TrackWise
eDMS
SFLMS

Job description

Manpower Staffing Services (Singapore) Pte Ltd invites applications for a QA Specialist role focusing on GMP-compliant QMS, document control, training, supplier management, and CAPA. You will ensure data integrity and support continuous improvement within cGMP standards at our Jurong facility.

The contract position requires 1-3 years in pharmaceutical quality, familiarity with TrackWise or similar QMS, and strong collaboration across teams to uphold regulatory commitments and client expectations.

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