Technical Writer II (Microbiology)

SGS; Muntinlupa; On-site; PHP 360,000 - 480,000; Full time

Job summary

SGS in Metro Manila seeks a Technical Writer (Level I) to compile accurate scientific reports from validated data. You will verify data across analytical instruments, execute test scripts for software re-validation, and assist in preparing SOPs and forms.

Strong English and pharma familiarity are preferred. Bachelor’s degree in chemistry required with at least 2 years in scientific data entry and report creation; knowledge of cGMP/ICH is a plus.

Qualifications

• Bachelor’s degree in chemistry or related science field.
• Minimum 2 years in scientific data entry and report creation, pharma setting preferred.
• Knowledge of cGMP and ICH guidelines is desired.
• Strong written and verbal English communication.

Responsibilities

• Compile scientific reports from validated data and follow internal templates.
• Crosscheck data consistency across analytical techniques and report anomalies.
• Execute predefined test scripts for software re-validation and document results.
• Assist in revision and approval of SOPs, worksheets, and forms.
• Ensure compliance with SGS integrity, QHSE, and HR policies.

Skills

Scientific report writing

Data validation

Time management

Attention to detail

English proficiency

Education

Bachelor’s degree in chemistry or related science field

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

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.

Job Description

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.