QA Coordinator (Contractor)

Pfizer Inc; Saudi Arabia; On-site; SAR 120,000 - 150,000; Full time

Job summary

Join a leading pharmaceutical company as a Quality Assurance Coordinator, where you will ensure compliance with quality standards through batch records review and validation activities. This role requires a Bachelor's degree in Pharmacy and offers an opportunity to make a significant impact on patient care. Ideal candidates will have strong communication skills and a collaborative mindset.

Qualifications

• Minimum Bachelor's degree in Pharmacy.
• Ability to work in teams and communicate effectively.
• Experience at a manufacturing site is a plus.

Responsibilities

• Review and approve batch documentation following GMP rules.
• Conduct process validation and develop validation protocols.
• Support daily activities in the Quality Assurance department.

Skills

Team Collaboration

Effective Communication

Problem-Solving

Time Management

Education

Bachelor's degree in Pharmacy or related field

Job description

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 (Quality Assurance Coordinator - Contractor), you will:

Batch Records Review and Release Activities:

• Follow up and review of batch documentation and assure strict adherence to written procedures.
• Follow up applying of GMP rules during review of batch documentation.
• Batch Record Review and Archiving.
• Products finished goods approval on Pfizer ERP (Enterprise Resource Planning) system.
• Review and approval of Master Batch Records.
• Release of finished goods on RSD SFDA DTTS (Drug Track & Trace System).

Execution and reporting of validation / qualification activities:

• Process Validation
• Cleaning Validation
• Packaging Validation
• Computerized System Validation
• Equipment Qualification
• Utilities Qualification (HVAC, purified water system, compressed air)
• Development of relevant Validation Master Plans and SOPs.
• Development of Validation Protocols and Reports.
• Process verification.
• Equipment/systems Validation periodic review.

Support in Quality Assurance department daily activities and tasks

Here Is What You Need (Minimum Requirements)

• Bachelor's degree in Pharmacy or related field.
• Ability to work effectively in a team environment, both within one's own team and interdepartmental teams
• Effective written and oral communication skills

Bonus Points If You Have (Preferred Requirements)

• Experience at a manufacturing site.
• Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis, and change control management
• Strong problem-solving skills
• Ability to work independently and as part of a team
• Excellent time management and multitasking abilities

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