Overview
Quality Assurance Technician Jobs in County Carlow, Ireland at Independent Solutions
Title: Quality Assurance Technician
Company: Independent Solutions
Location: County Carlow, Ireland
Quality Assurance Technician
Location: Carlow, Ireland
Work Model: Fully Onsite (Shift Role)
Overview
We are seeking a Quality Technician to support manufacturing operations within a GMP-regulated pharmaceutical environment. This role involves working closely with production teams to ensure compliance with quality standards, regulatory requirements, and continuous audit readiness.
Experience in a quality function and/or aseptic (sterile) manufacturing environment is highly beneficial.
Key Responsibilities
- Work on a 4-cycle shift pattern (12-hour shifts).
- Perform timely review of batch documentation (EBRs), investigations, and reports.
- Identify and escalate quality concerns, supporting resolution activities.
- Respond effectively to unplanned events and technical issues.
- Support shop-floor quality activities, including line clearances and walk-throughs.
- Contribute to customer complaint investigations where required.
- Monitor and report Right First Time (RFT) and audit readiness metrics.
- Ensure compliance with cGMP, GDP, and regulatory requirements (EU & US).
- Collaborate cross-functionally to drive quality improvements.
Additional Responsibilities
- Provide quality support to production teams (IPT).
- Assist with batch record review, line clearances, and deviation resolution.
- Work with cross-functional teams to maintain and improve GMP standards.
- Comply with Quality, Manufacturing, and EHS systems and procedures.
- Utilize computerized systems (e.g. SAP, MES, Trackwise) in daily tasks.
Qualifications & Experience
Education:
- Bachelor’s degree (or higher) in a Science-related discipline preferred.
Experience:
- 3 years’ experience in a QA/QC role within pharmaceutical manufacturing.
- Experience in aseptic/sterile manufacturing is desirable.
- Exposure to SAP, MES, Trackwise or similar systems preferred.
Skills & Knowledge:
- Strong understanding of cGMP, GDP, and regulatory requirements.
- Experience with batch record review, deviations, CAPA, and investigations.
- Ability to manage multiple tasks and work in a fast-paced environment.
- Strong documentation, communication, and problem-solving skills.
Additional Information
- Fully onsite role (no remote/hybrid option)
- Shift premium: +33%
- Prior experience in shift work, QA, or aseptic environments is advantageous
