Pharma Technical Writer: GMP Reports & Validation (Hybrid)

SGS; Muntinlupa; Hybrid; PHP 480,000 - 720,000; Full time

Job summary

SGS Global Business Solutions in the Philippines seeks a Technical Writer (Level I) to compile accurate scientific reports from validated data, verify consistency across analytical techniques, and report discrepancies. You will also execute predefined test scripts for software re-validation and support SOP and worksheet development.

You will assist in the revision and approval of department SOPs, testing worksheets, and forms, ensuring compliance with SGS policies and industry standards.

Qualifications

• Bachelor's degree in chemistry or related science; pharma experience preferred.
• Minimum 2 years of relevant scientific data entry and report creation experience.
• Good understanding of cGMP and regulatory guidelines (ICH, EP, USP).

Responsibilities

• Compile scientific reports from validated data and ensure data consistency across techniques.
• Execute predefined test scripts for software re-validation and document results.
• Assist in revision, creation, review and approval of SOPs, worksheets and forms.
• Document findings using standardized report templates and communicate updates.

Skills

English proficiency

Microsoft Office

Interpersonal skills

Time management

Attention to detail

Independent / collaborative work

Education

Bachelor's degree in chemistry or related science

Tools

Microsoft Office Suite

Job description

SGS Global Business Solutions in the Philippines seeks a Technical Writer (Level I) to compile accurate scientific reports from validated data, verify consistency across analytical techniques, and report discrepancies. You will also execute predefined test scripts for software re-validation and support SOP and worksheet development.

You will assist in the revision and approval of department SOPs, testing worksheets, and forms, ensuring compliance with SGS policies and industry standards.