QA Specialist

QCS Staffing Ltd; Dublin; On-site; EUR 50,000 - 70,000; Part time

Job summary

QCS Staffing Ltd, on behalf of a global leader in the life sciences sector, seeks a QA Specialist to support Dublin operations on an initial 11-month contract. The role focuses on quality oversight for introduction of new equipment and validation activities.

You will conduct quality reviews of engineering commissioning and qualification activities, support deviation investigations, and oversee change controls related to new equipment, ensuring compliance with Irish, European, and international

Qualifications

• Extensive experience in a quality role, ideally in a pharmaceutical manufacturing environment.
• Bachelor’s degree or higher in a related Science discipline (preferred).
• Knowledge of regulatory/code requirements related to Irish, European, and International Codes, Standards, and Practices.

Responsibilities

• Provide quality oversight and direction for the introduction of new equipment up to and including validation activities.
• Conduct quality reviews and approvals of engineering/ commissioning and qualification activities.
• Conduct quality reviews and approvals of validation/automation/utilities activities.
• Support deviation investigations and close out in a timely manner.
• Quality oversite of Change controls related to introduction, commissioning and qualification of new equipment.

Skills

Quality oversight

Validation activities

Change controls

Deviation investigations

Education

Bachelor’s degree or higher in related Science discipline

Job description

QA Specialist – Dublin, Ireland – Initial 11-Month Contract – Life Sciences

Our client is a global leader in pharmaceutical innovation, specialising in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced QA Specialist to support their dynamic team and drive forward groundbreaking projects in Dublin.

What You’ll Deliver

• Provide quality oversight and direction for the introduction of new equipment up to and including validation activities.
• Conduct quality reviews and approvals of engineering/ commissioning and qualification activities.
• Conduct quality reviews and approvals of validation/automation/utilities activities.
• Support deviation Investigations and close out in a timely manner.
• Quality oversite of Change controls related to introduction, commissioning and qualification of new equipment.

What you’ll need

• Extensive experience in a quality role, ideally in a pharmaceutical manufacturing environment.
• A bachelor’s degree or higher in a related Science discipline is preferred.
• Extensive experience in a quality role, ideally in a pharmaceutical manufacturing environment.
• Knowledge of regulatory/code requirements related to Irish, European, and International Codes, Standards, and Practices.