SOQ HUB Senior Associate

Pfizer, S.A. de C.V; Makati; On-site; PHP 400,000 - 600,000; Full time

Job summary

A leading pharmaceutical company in Metro Manila is seeking a Quality Assurance professional to evaluate drug batches and ensure compliance with regulatory standards. The ideal candidate has a solid understanding of Good Manufacturing Practices and at least 2 years of relevant experience. Join us in our mission to deliver safe and effective products to patients.

Benefits

Competitive compensation

Benefits programs

Qualifications

• Solid understanding of current Good Manufacturing Practices and relevant GxP regulations.
• Experience in quality administered systems preferred.
• Ability to mentor and guide other colleagues.

Responsibilities

• Evaluate and review clinical and commercial drug batches.
• Conduct sampling and statistical process control procedures.
• Approve investigations and change control activities.

Skills

Strong critical thinking

Proactive problem-solving

Effective teamwork

Good knowledge of Microsoft Excel and Word

Education

High school diploma with 8+ years of experience

Associate’s degree with 6+ years of experience

BA/BS with 2+ years of experience

MBA/MS with any years of relevant experience

Job description

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

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.

Job Description

What You Will Achieve

In this role, you will:

• Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
• Conduct rigorous sampling and statistical process control procedures to identify deviations from standards.
• Approve investigations and change control activities to maintain compliance with configuration management policies.
• Contribute to moderately complex projects, managing time effectively and developing short-term work plans.
• Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts.
• Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
• Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

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 current Good Manufacturing Practices and relevant GxP regulations and standards
• Strong critical thinking skills
• Ability to work effectively within own team and interdepartmental teams
• Good working knowledge of Microsoft Excel and Word
• Proactive approach to problem-solving

Bonus Points If You Have (Preferred Requirements)

• Experience in quality administered systems
• Strong organizational skills and attention to detail
• Experience with regulatory compliance and documentation
• Ability to mentor and review the work of other colleagues

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