Technical Writer II (Pharma)

TL;DR

Technical Writer II (Pharma): Compiling accurate scientific reports and documentation for laboratory analytical data with an accent on data consistency and regulatory compliance. Focus on executing software re-validation scripts, maintaining SOPs, and ensuring adherence to cGMP/GcLP standards.

Location: Must be based in Muntinlupa, Philippines

Company

hirify.global is the world’s leading testing, inspection, and certification company, recognized as the global benchmark for quality and integrity.

What you will do

• Compile scientific reports using validated data from analytical instruments.
• Verify data consistency across analytical techniques and report discrepancies.
• Execute predefined test scripts for software re-validation and document outputs.
• Create, review, and approve department SOPs, testing worksheets, and forms.
• Monitor and document updates to compendia like EP and USP.
• Perform spreadsheet validations according to internal SOPs.

Requirements

• Bachelor’s degree in chemistry, pharmacy, or a related science field.
• Minimum 2 years of relevant experience in scientific data entry or laboratory testing within a pharma setting.
• Demonstrated understanding of cGMP and/or GcLP regulations.
• Strong command of English (B2 minimum) with excellent written communication skills.
• Proficiency in Microsoft Office Suite.
• Meticulous attention to detail and strong time management skills.

Nice to have

• Understanding of analytical methods.
• Knowledge of regulatory guides such as ICH M10 and pharmacopeias (EP, USP).

Culture & Benefits

• Opportunity to work within a global network of laboratories and offices.
• Commitment to professional training and development.
• Adherence to a strong Code of Integrity and Professional Conduct.