Technical Writer (Pharma)

Location: Alabang, Muntinlupa, Metro Manila, Philippines; onsite for the first 3 months, then transitioning to a hybrid setup

Company

A global testing, inspection, and certification organization focused on quality, integrity, and scientific services.

What you will do

• Compile validated data from analytical instruments into accurate, structured scientific reports.
• Cross-check results across analytical techniques and report anomalies or data discrepancies.
• Execute predefined software revalidation test scripts, document outputs, and perform retesting after updates.
• Write, review, and support approval of SOPs, testing worksheets, protocols, reports, and forms.
• Review updates to EP and USP compendia and communicate relevant changes to departments.
• Perform spreadsheet validations and maintain compliance with quality, health, safety, and environmental procedures.

Requirements

• Bachelor’s degree in chemistry, pharmacy, or a related scientific field.
• At least 2 years of relevant experience in scientific data entry, report creation, or laboratory testing within a pharmaceutical setting.
• Understanding of cGMP and/or GLP regulations, analytical methods, ICH M10, and pharmacopeias such as EP and USP.
• English proficiency at B2 level or higher, with strong verbal and written communication skills.
• Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
• Strong attention to detail, time management, interpersonal, collaboration, and independent working skills.

Culture & Benefits

• Three-month onsite work arrangement followed by hybrid work.
• Work in a global business solutions center supporting scientific and laboratory operations.
• Opportunities for professional training, education, and development.
• Work within established integrity, quality, health, safety, environmental, and HR policies.