Senior Tech Transfer Lead - Pharma Manufacturing

Pfizer; Hinoba-an; On-site; PHP 800,000 - 1,000,000; Full time

Benefits offered by this job

Equal opportunity employer

On-site work availability

Job summary

Pfizer is seeking a qualified engineer to lead technology transfer and validation efforts for new molecules, handling exhibit batches and regulatory submissions. You will evaluate validation master plans and protocols, troubleshoot issues, and perform data analysis to support quality investigations.

The role requires strong knowledge of GMP, quality systems, and cross-functional collaboration, with on-premise work at Pfizer facilities in the Philippines.

Qualifications

• High school diploma or equivalent with 8+ years of experience, or an Associate’s degree with 6+ years, or a BA/BS with 2+ years, or MBA/MS with any years of relevant experience.
• Experience in tech transfer processes, scale-ups, exhibit batches and process validations.
• Familiarity with FDA regulations, GMP quality systems, and information systems such as document management and QA tracking.

Responsibilities

• Lead tech transfer for new molecules and exhibit batches.
• Evaluate, review and approve validation master plans, protocols and reports.
• Troubleshoot validation issues for equipment and processes.
• Perform statistical analysis of testing results and support Quality Investigations.
• Coordinate testing with functional groups and contribute to regulatory submissions.

Skills

Tech transfer

Validation

Quality systems

Statistical analysis

Regulatory submissions

Education

High school diploma + 8+ years experience

Associate’s degree + 6+ years experience

BA/BS + 2+ years experience

MBA/MS + any years experience

Tools

Global Document Management System

SAP (System Applications & Products)

Quality Tracking System

Job description

Pfizer is seeking a qualified engineer to lead technology transfer and validation efforts for new molecules, handling exhibit batches and regulatory submissions. You will evaluate validation master plans and protocols, troubleshoot issues, and perform data analysis to support quality investigations.

The role requires strong knowledge of GMP, quality systems, and cross-functional collaboration, with on-premise work at Pfizer facilities in the Philippines.