Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.

What You Will Achieve

In this role, you will:

Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.

Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.

Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.

Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.

Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.

Manage routine quality systems such as Change Control, Documentation, and Investigations, and coordinate testing with functional groups.

Maintain the Site Validation Master Plan, support regulatory audits, and represent validation on site or network teams.

Support product transfers/new product development, regulatory queries, and cost improvement projects.

Ensuring integration of validation schedules in production and participating in deviation investigations.

Maintain and manage of Continued process verification (CPV) and Periodic Cleaning Monitoring (PCM)

Here Is What You Need (Minimum Requirements)

You hold a degree in pharmacy, pharmaceutical technology or comparable scientific discipline.

Minimum two years of experience in pharmaceutical industries combined with strong knowledge of regulatory requirements, GMP, and pharmaceutical development processes.

Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems

Excellent verbal and written communication skills

Ability to work independently and in a team environment

Ability to work under pressure and adapt to a fast-paced environment

Strong analytical and problem-solving skills

Strong organizational and time management skills

Willing to be placed in Jakarta

Bonus Points If You Have

Strong working knowledge of various quality systems and processes

Ability to mentor and guide other colleagues

Experience with Solid Oral Dosage/Semi-Solid Dosage/Liquids Dosage forms

Lean Six Sigma Yellow Belt or Green Belt certification

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control