Quality Specialist

CPi Technology Ltd; Cork; On-site; EUR 55,000 - 75,000; Full time

Benefits offered by this job

Health scheme

Pension plan

Career advancement

Dynamic environment

On-site parking

EV charging

Flexible working

Job summary

CPi Technology Ltd. is seeking a Quality Specialist to join our growing team in Little Island, Cork. The role sits at the heart of maintaining quality and safety for our bio/pharmaceutical customers, ensuring QMS compliance and supply chain integrity.

You will collaborate cross-functionally under the Quality Lead, contributing to audits, CAPA and change control while supporting continuous improvement and regulatory readiness in an ISO‑certified environment.

Qualifications

• 3+ years in a GMP/regulated quality role.
• Experience with bio/pharma, medical devices, nutraceuticals or food science.
• Bachelor’s degree or graduate in science, engineering or technology.
• Authorized to work in Ireland.

Responsibilities

• Drafting and timely execution of actions for Change Control and CAPA.
• Batch record review and material release to ensure GMP compliance.
• QA review and approval of SOPs, work instructions and forms.
• Execution of internal and external audits.
• Product release activities.
• Continuous improvement initiatives.
• Contribution to improving KPI metrics.
• Update of key tracking tools for QMS.

Skills

Quality function experience (GMP)

Education

Science/Engineering/Technology degree

Job description

Job Description

We are looking to recruit a Quality Specialist to join our expanding team. The position is permanent and is site‑based in our Headquarters, in Little Island, Cork. The successful candidate would be joining the company at a key and exciting time in the company’s growth as we expand our operations and customer base.

About the Role

Reporting to the Quality Lead, this position requires an effective collaborator to work cross-functionally and as part of a team. With a strong focus on supplier and customer management, this role will facilitate continuing compliance with the QMS. Working in an ISO-certified environment, CPi endeavours to excel by also matching cGXP guidelines through shared ownership and execution of the QMS. This role is key to maintaining the quality and safety of products for the bio/pharmaceutical market, ensuring the company meets the specification requirements of its multinational customers, and assuring the security of the supply chain and the company’s interests.

Key Responsibilities

• Drafting and timely execution of actions for Change Control and CAPA Update of key tracking tools for QMS
• Batch Record Review and material release (including CoA) to ensure compliance with GMP requirements
• QA Review and Approval of SOPs, Work Instructions, and Forms
• Execution of internal and external audits
• Product release activities
• Continuous improvement initiatives
• Contribution to improving KPI metrics
• Update of key tracking tools for QMS

Experience & Qualifications/Requirements

• 3 years+ in a Quality function in a GMP/regulated environment
• Bio/Pharmaceutical, Medical Device, Nutraceutical, or Food Science background
• Bachelor’s degree/Graduate with a scientific degree or qualifications in science, engineering, or technology
• Exposure to customer/regulatory audits
• Prior experience of system ownership
• Candidate must also be authorized to work in Ireland

Benefits

• Competitive salary and benefits package, including Company Health Scheme and Pension Plan
• Opportunities for career advancement in a rapidly expanding company
• A dynamic, supportive work environment with a focus on professional growth
• Sports & Social Club
• On-site parking, including access to EV Charging
• Flexible working arrangements

If you’re a self-motivated, detail-oriented individual with a desire to contribute to the growth of an innovative Irish biotech company, we encourage you to apply today.