QA Oversight & Packaging Development Specialist

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, 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. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.

What You Will Achieve

In this role, you will:

Prepare and review artwork, circulate artwork to the respective approvers, and communicate with supplier or manufacturer if there is any revision through Pfizer system.

Prepare Packaging Material Specification.

Support activities related to Packaging Material Development

Update and maintain QA documentation/ database and SOPs

Update and maintain the Master Packaging Line for standard in packaging line inspection.

Manage QA Visual board for Artwork activities area to ensure QA operations performance deliverable

Updating QA’s Standard Operating Procedure (SOP)/ Prosedur Tetap (PROTAP) in accordance with actual practices, Pfizer Standards, current GMP, and regulatory requirements, and ensure that all QA’s procedures are consistently followed and implemented.

Support self-inspection and other audits as scheduled.

Support all other QA activities such as manufacturing and packaging oversight, provide data for annual product review, quality metric and maintain the database of QA metrics.

Here Is What You Need (Minimum Requirements)

Bachelor degree with relevant 2- 4-years of work experience, or Bachelor degree of Pharmacy with relevant experience.

Able to demonstrate artwork-editing skills as per requested.

Understanding of current Good Manufacturing Practices (part of GxP)

Fluency in English with effective written and verbal communication skills

This role will be direct contract based (fixed term)

Bonus Points If You Have (Preferred Requirements)

Relevant experience at a Pharmaceutical manufacturing site.

Experience in managing changes of process.

Able to create documented reports for non-conformance and deviations

Excellent time management and multitasking abilities

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

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