This role has a fixed term period of 12 months.

Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

Contribute to moderately complex projects by managing your time effectively and planning short-term work activities.
Engage with stakeholders to address product quality complaints and ensure compliance with GMP/GDP during audits and inspections.
Lead product quality investigations and follow up on actions to resolve compliance issues in the marketplace.
Serve as a Subject Matter Expert and reviewer for Standard Operating Procedures (SOPs) and analyze inquiry data to identify trends.
Assist with audit Corrective & Preventive Actions (CAPAs), review documentation related to repackaging and relabeling, compile Key Performance Indicator figures, and facilitate product-focused training sessions.

Here Is What You Need (Minimum Requirements)

High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
Solid understanding of regulatory GDP/GMP compliance issues related to the manufacturing and distribution of medicinal products
Excellent organizational skills and the ability to juggle multiple priorities
Strong collaboration, communication, and interpersonal skills to work effectively with local, regional, and global colleagues

This role has a fixed term period of 12 months.

Use Your Power for Purpose

What You Will Achieve

In this role, you will:

Contribute to moderately complex projects by managing your time effectively and planning short-term work activities.
Engage with stakeholders to address product quality complaints and ensure compliance with GMP/GDP during audits and inspections.
Lead product quality investigations and follow up on actions to resolve compliance issues in the marketplace.
Serve as a Subject Matter Expert and reviewer for Standard Operating Procedures (SOPs) and analyze inquiry data to identify trends.
Assist with audit Corrective & Preventive Actions (CAPAs), review documentation related to repackaging and relabeling, compile Key Performance Indicator figures, and facilitate product-focused training sessions.

Here Is What You Need (Minimum Requirements)

High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
Solid understanding of regulatory GDP/GMP compliance issues related to the manufacturing and distribution of medicinal products
Excellent organizational skills and the ability to juggle multiple priorities
Strong collaboration, communication, and interpersonal skills to work effectively with local, regional, and global colleagues

Supply Operations Quality Associate

Supply Operations Quality Associate

Pfizer

Pfizer

Benefits

Pfizer