Manager, Quality Control

EyeBio; Carlow; Hybrid; EUR 70,000 - 100,000; Full time

Job summary

EyeBio in Carlow is seeking a Quality Control Manager to oversee manufacturing quality and compliance at our Carlow site. You will lead data integrity, GMP adherence, and batch release activities while guiding a high-performing team.

The role requires 5+ years in pharma, people management, and a strong commitment to quality systems and regulatory requirements, with a hybrid working model supporting office-based and site activities.

Qualifications

• Bachelor's degree in Engineering or Science.
• 5+ years of pharma industry experience.
• People management experience.

Responsibilities

• Ensure data integrity and complete GMP training.
• Escalate GMP violations affecting product safety, quality, or purity.
• Provide training to team members and foster a safe, compliant culture.
• Support quality reporting and cover for the Associate Director, Quality Control.
• Ensure batch testing, review, release, and product disposition processes.
• Resolve quality issues with compliance guidance and lifecycle controls.
• Conduct and approve laboratory testing, material inspections, and method validation.
• Manage CAPA activities, quality agreements, and risk management per policies.

Skills

BioAssay

GMP

Quality Control

Quality Management

Regulatory Requirements

Education

Bachelor's Degree in Engineering or Science

Job description

Job Description

We are excited to announce a new opportunity at our Carlow Site for a Quality Control Manager. As a Quality Control Manager, the successful candidate will play a pivotal role in ensuring the highest standards of quality and compliance in our manufacturing processes.

Bring energy, knowledge, innovation to carry out the following:

• You will ensure adherence to data integrity principles (Attributable, Legible, Contemporaneous, Original, and Accurate) and complete applicable Current Good Manufacturing Practice training.
• Escalate potential Current Good Manufacturing Practice violations and concerns affecting product safety, efficacy, quality, or purity.
• Provide training to team members and foster a safe, compliant, and high-performing culture through collaboration.
• Support quality reporting improvements and step in for the Associate Director, Quality Control during absences.
• You will ensure processes for batch testing, review, release, and product disposition are followed.
• Resolve quality issues with compliance guidance and support material/product lifecycle controls and procedures.
• Conduct, review, and approve laboratory testing, material inspections, and validation of laboratory methods.
• You’ll manage Corrective and Preventive Actions activities, quality agreements, and risk management processes, ensuring compliance with regulatory requirements and divisional Quality Management System policies.

What Skill You Will Bring to the Team

• Bachelors Degree in Engineering or Science
• You bring 5+ years of experience in the pharma industry.
• People management experience

Our facility in Carlow site broke ground in 2008 and is a filling site for the launch and commercial supply of vaccines, biologics and small molecule drug product. Since its initial launch, the site has attracted significant internal investment and is now home to a number of state-of-the-art production facilities, laboratories and temperature-controlled warehousing units. The Carlow site is a significant employer in the South East region and attracts high performing talent through close collaborations with universities and colleges in the region

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Required Skills:

BioAssay, Good Manufacturing Practices (GMP), Quality Control (QC), Quality Management, Regulatory Requirements

Preferred Skills:

Collaboration

Employee Status:

Regular

Flexible Work Arrangements:

Not Applicable

Job Posting End Date:

09/10/2026