Quality Auditor

Occupli Limited; Dublin; On-site; EUR 60,000 - 80,000; Full time

Job summary

A leading quality management firm in Dublin is seeking a Quality Auditor to enhance their quality and compliance initiatives. The role requires a bachelor's degree and over 5 years of experience in Quality Assurance within regulated environments. Candidates must have a strong grasp of GMP principles and be adept at collaboration across various teams. This position offers career development opportunities within a dynamic environment focused on innovation and excellence.

Qualifications

• Minimum 5 years' experience in Quality Assurance, Quality Control, or Technical Operations in a regulated industry.
• At least 2 years' experience performing release or quality review functions in a GMP environment.
• Strong understanding of qualification processes and raw material management.

Responsibilities

• Support quality activities across site and cross-functional teams.
• Review and approve documentation including CAPAs and investigations.
• Collaborate with stakeholders on quality documentation.

Skills

Proactive and results-driven approach

Excellent collaboration skills

Strong communication skills

Strong attention to detail

Ability to manage multiple priorities

Commitment to continuous improvement

Education

Bachelor’s degree in Chemistry, Biology, Engineering, or Supply Chain

Tools

SAP

Veeva

Electronic documentation platforms

Job description

Dublin 17, Ireland | Posted on 15/10/2025

At Occupli, we are driven by a commitment to excellence, integrity, and innovation. The Quality Auditor will play a key role in supporting quality and compliance initiatives across the organization, ensuring that products, processes, and systems consistently meet regulatory standards and customer expectations.

This position is suited to an experienced quality professional with a strong understanding of GMP principles and cross-functional collaboration in a technical or manufacturing environment.

Key Responsibilities

• Support quality activities across site and cross-functional teams within the organization.
• Review and approve documentation including CAPAs, change controls, investigations, and related reports.
• Manage quality aspects of material and supplier management, including preparation of qualification documentation, supplier audit follow-up, and maintenance of supplier records.
• Collaborate with stakeholders such as QC, Engineering, Technical Operations, and Supply Chain in developing and reviewing quality documentation throughout the product lifecycle.
• Review and approve GMP documentation for completeness and accuracy.
• Partner with cross-functional teams to ensure timely delivery of project milestones and quality deliverables.
• Contribute to continuous improvement initiatives, identifying and implementing actions that enhance quality systems and operational efficiency.

Qualifications & Experience

• Bachelor’s degree (or higher) in a relevant discipline such as Chemistry, Biology, Engineering, or Supply Chain.
• Minimum of 5 years’ experience in Quality Assurance, Quality Control, or Technical Operations within a regulated industry such as pharmaceutical, biotech, or medical devices.
• At least 2 years’ experience performing release or quality review functions in a GMP environment.
• Strong understanding of qualification processes, single-use systems, and raw material management in a regulated setting.
• Up-to-date knowledge of current GMP regulations and industry trends.
• Experience with quality systems such as SAP, Veeva, or electronic documentation platforms is an advantage.

Skills & Attributes

• Self-starter with a proactive and results-driven approach.
• Excellent collaboration, communication, and organizational skills.
• Strong attention to detail with the ability to manage multiple priorities.
• Demonstrated ability to influence and support cross-functional teams.
• Commitment to continuous improvement and professional excellence.