Anter Consulting Pte. Ltd. · MyCareersFuture · 1w
QA Specialist – Documentation
Singapore- Posted
- 2026-09-30 (1w)
- Place
- Singapore
- Commitment
- Contract
- Salary
- SGD 4,000 – 6,000 / month
- Experience
- 2+ YOE
- Department
- Healthcare / Pharmaceutical
- Source
- MyCareersFuture (the employer’s own listing)
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Skills in this posting
External Audit
We are seeking a QA Specialist – Documentation to support GMP document management within a pharmaceutical manufacturing environment. The role involves maintaining controlled documentation, supporting digital documentation initiatives and ensuring records remain accurate, compliant and readily retrievable.
Responsibilities
• Maintain document management processes in accordance with company quality standards and applicable regulatory requirements.
• Support the implementation of electronic logbooks and electronic forms.
• Manage the GMP governance and issuance of paper-bound logbooks and controlled printing of forms.
• Perform document archival and scanning for electronic storage.
• Manage the GxP documentation lifecycle, including document creation, revision and obsolescence.
• Coordinate with departments and subject matter experts to ensure documentation accurately reflects business processes and meets regulatory and quality requirements.
• Review documents for accuracy, completeness, clarity, grammar and consistency with established writing standards.
• Identify and reduce unnecessary duplication within documentation.
• Collect requests for documentation changes, prioritise updates and coordinate their completion.
• Ensure documents undergo regular review and remain current.
• Maintain appropriate document distribution and access controls in accordance with information classification requirements.
• Support internal and external audits and inspections by ensuring required documents are current and readily retrievable.
Requirements
• Minimum 2 years of relevant experience, preferably in Manufacturing, Validation or Quality within the pharmaceutical or biotechnology industry.
• Experience in vaccines and/or biologics manufacturing is preferred.
• Good understanding of pharmaceutical regulations, quality standards, GMP/GxP documentation practices and data integrity requirements.
• Strong attention to detail and the ability to maintain accurate and compliant records.
• A disciplined approach to decision-making, task prioritisation and execution.
• Good communication and interpersonal skills, with the ability to collaborate across departments and promote a quality-focused culture.
• Fluent in spoken and written English.
Anter Consulting Pte. Ltd.
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