R&D Technical Writer (Pharmacuetical)

SmartRecruiters, Inc.; Muntinlupa; Hybrid; PHP 650,000 - 900,000; Full time

Job summary

SGS is seeking a Technical Writer (Level I) for its Global Business Solutions center. You will compile scientific reports from validated instrument data and verify cross-technique consistency. You will also run predefined software revalidation tests and assist in SOP/document revision processes.

The role requires a chemistry degree, 2+ years in scientific data entry/reporting, and knowledge of cGMP/GxLP; onsite for 3 months, then transitioning to a hybrid work setup.

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).
• Demonstrated understanding of cGMP and/or GcLP regulations is required.
• Good understanding of analytical methods; knowledge of regulatory guides such as ICH M10, EP, USP is preferred.

Responsibilities

• Compile scientific reports using validated data from analytical instruments; produce high-quality documentation.
• Crosscheck data across techniques to ensure results are consistent before finalizing reports.
• Execute predefined test scripts for software revalidation and document outputs.
• Document analytical findings in standardized report templates.
• Review EP/USP updates and communicate changes to relevant departments.

Skills

English proficiency

Interpersonal skills

Time management

Attention to detail

Independent work

Education

Bachelor's degree in Chemistry

Tools

Microsoft Office Suite

Job description

We are SGS – the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for quality and integrity. Our 93,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

Primary Responsibilities

• As a member of the team in our Global Business Solutions (GBS) center, the Technical Writer (Level I) will be responsible for compiling accurate scientific reports using validated data from analytical instruments. Verify data consistency across techniques, identify and report discrepancies.
• Additionally, execute predefined test script for regular software re-validation, and report test outputs.
• Assist in the revision, creation, review and approval process for appropriate department SOPs, testing worksheets, and forms.

Qualifications

Specific Responsibilities

• Compile scientific reports using validated data from various analytical instruments. Produce clear, structured, high‑quality documentation following scientific conventions and internal templates.
• Crosscheck and verify data consistency across different analytical techniques to ensure results logically correspond before report finalization. Report on anomalies in the outputs.
• Execute predefined test scripts as part of scheduled software revalidation activities, accurately documenting and reporting all resulting outputs. Identify and report discrepancies observed during testing. Perform retesting once updates have been applied.
• Document analytical findings by compiling data into standardized report templates.
• Review the compendia updates (e.g., EP, USP), document changes, and communicate updates to relevant departments.
• Assists with writing and reviewing testing worksheets, protocols and reports. Ensure approval for department SOPs, worksheets, and forms. Perform spreadsheet validations according to SOP.
• Performs other related duties as may be assigned either in support of departmental goals or for his/her personal or professional training, education or development as programmed by his/her immediate superior.
• At all times, comply with SGS Code of Integrity and Professional Conduct and with all SGS QHSE and HR policies and procedures. Ensure the work area in GBS is always clean and presentable.

Profile

• 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 all regulatory guides such as ICH M10, pharmacopeias (EP, USP), preferrable.

Additional Information

Required Skills

• Strong command of the English language (B2 as minimum), with good verbal- and written communication skills (grammar and composition).
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook).
• Strong interpersonal skills and the ability to work both collaboratively and independently.
• Proven time management skills and meticulous attention to detail.
• Work arrangement of3 months onsite, transitioning to a hybrid setup thereafter.