QA Chemist: GxP Compliance & Quality Investigator

Pfizer; Cork; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

Pfizer in Ringaskiddy, Cork is seeking a QA Chemist to evaluate clinical and commercial drug batches for compliance with specifications and regulatory standards. You will perform sampling, statistical process control, and approve investigations and change controls to maintain cGMP.

The role requires strong problem-solving, attention to detail, and collaboration across teams. The position focuses on regulatory compliance with GxP, documentation oversight, and continuous quality improvements in a

Qualifications

• Experience with current Good Manufacturing Practices (GxP) and related regulations.
• Ability to review and approve investigations and change controls.
• Ability to mentor and review colleagues’ work.
• Experience using AI tools to support problem solving and productivity.

Responsibilities

• Evaluate and review clinical and commercial drug batches for compliance with specs.
• Conduct sampling and statistical process control to identify deviations.
• Approve investigations and change control activities to maintain compliance.
• Contribute to projects and develop short-term work plans, managing time effectively.
• Independently assess Change Control activities for GxP impacts.
• Investigate and document Quality Assurance deviations and escalate as needed.
• Ensure regulatory compliance with GxP and oversee site documentation.

Skills

Quality mindset

Critical thinking

Problem solving

Teamwork

Attention to detail

Education

High school diploma

Associate’s degree

Bachelor’s degree in a related field

MBA/MS with relevant experience

Tools

Microsoft Excel

Microsoft Word

Job description

Pfizer in Ringaskiddy, Cork is seeking a QA Chemist to evaluate clinical and commercial drug batches for compliance with specifications and regulatory standards. You will perform sampling, statistical process control, and approve investigations and change controls to maintain cGMP.

The role requires strong problem-solving, attention to detail, and collaboration across teams. The position focuses on regulatory compliance with GxP, documentation oversight, and continuous quality improvements in a