Pharma Documentation Engineer - Quality & Compliance

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD.; Singapore; On-site; SGD 70,000 - 100,000; Full time

Job summary

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. is seeking a qualified engineering professional in Singapore to develop and manage comprehensive documentation for site operations, including SOPs, quality standards, and qualification protocols.

The role requires familiarity with cGMP practices and regulatory expectations such as HSA and FDA. The ideal candidate will support engineering operations for manufacturing, utilities and facilities, coordinate project documentation, and handle ad-hoc tasks

Qualifications

• Good technical writing skills.
• Experience drafting SOPs, quality standards and qualification protocols (URS, DQ, IQ, OQ, PQ).
• Familiar with cGMP practices and regulatory requirements (e.g., HSA, FDA).

Responsibilities

• Develop and maintain engineering documentation for site, following QMS procedures.
• Support engineering operations for manufacturing, utilities and facilities projects (new and retrofit).
• Coordinate and manage project documentation.
• Assist with ad-hoc duties as assigned by supervisor.

Skills

Technical writing

Education

Engineering degree

Job description

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. is seeking a qualified engineering professional in Singapore to develop and manage comprehensive documentation for site operations, including SOPs, quality standards, and qualification protocols.

The role requires familiarity with cGMP practices and regulatory expectations such as HSA and FDA. The ideal candidate will support engineering operations for manufacturing, utilities and facilities, coordinate project documentation, and handle ad-hoc tasks