Scientific Documentation Specialist

Content Creators; Muntinlupa; Hybrid; PHP 360,000 - 540,000; Full time

Benefits offered by this job

Microsoft Office skills

Job summary

SGS is seeking a Technical Writer (Level I) in its Global Business Solutions center. You will compile accurate scientific reports using validated data from analytical instruments, verify data consistency, and report discrepancies. You will also execute predefined test scripts for software re-validation and support in SOPs, worksheets and forms.

The role requires a chemistry-related degree, 2+ years in pharma data/report work, familiarity with cGMP/ICh guidelines, and proficiency in MS Office.

Qualifications

• Bachelor’s degree in chemistry or a related science field (e.g. pharmacy).
• Minimum 2 years of relevant experience in scientific data entry and report creation and/or in laboratory testing, in pharma setting is required.
• Demonstrated understanding of cGMP and/or GcLP regulations is required.
• Good understanding of analytical methods, knowledgeable in regulatory guides such as ICH M10, EP, USP.

Responsibilities

• Compile scientific reports using validated data from analytical instruments, ensuring data consistency across techniques.
• Execute predefined test scripts for software re-validation and document outputs.
• Assist in revision, creation and approval of SOPs, testing worksheets, and forms.
• Review compendia updates (EP, USP) and communicate changes to departments.
• Assist with writing and reviewing worksheets, protocols and reports, ensuring SOP approvals.

Education

Bachelor’s degree in chemistry or related science

Tools

Microsoft Office Suite

Job description

SGS is seeking a Technical Writer (Level I) in its Global Business Solutions center. You will compile accurate scientific reports using validated data from analytical instruments, verify data consistency, and report discrepancies. You will also execute predefined test scripts for software re-validation and support in SOPs, worksheets and forms.

The role requires a chemistry-related degree, 2+ years in pharma data/report work, familiarity with cGMP/ICh guidelines, and proficiency in MS Office.