Pharma Documentation & GMP Compliance Engineer

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD.

is seeking a qualified documentation specialist to develop and maintain engineering documentation, SOPs, quality standards, and qualification protocols in line with site QMS procedures. The role requires familiarity with cGMP practices for pharmaceutical manufacturing, knowledge of regulatory requirements (HSA, FDA, etc.), and ability to coordinate project documentation for manufacturing, utilities and facilities, while supporting ad-hoc tasks from

Qualifications

• Degree in engineering and minimum of 5 years relevant experience.
• Strong ability to develop and maintain engineering documentation.
• Familiarity with cGMP practices in pharmaceutical manufacturing.

Responsibilities

• Develop SOPs, quality standards and qualification protocols (URS, DQ, IQ, OQ, PQ).
• Follow site QMS procedures to ensure compliant documentation.
• Support engineering operations for site projects (manufacturing, utilities & facilities).
• Coordinate project documentation and handle ad-hoc tasks from supervisor.

Skills

Technical writing

Document control

Education

Engineering degree

Job description

PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD.

is seeking a qualified documentation specialist to develop and maintain engineering documentation, SOPs, quality standards, and qualification protocols in line with site QMS procedures. The role requires familiarity with cGMP practices for pharmaceutical manufacturing, knowledge of regulatory requirements (HSA, FDA, etc.), and ability to coordinate project documentation for manufacturing, utilities and facilities, while supporting ad-hoc tasks from