QA Shift Lead: GMP, CAPA & Continuous Improvement

Bausch+Lomb

Waterford

On-site

EUR 45,000 - 65,000

Full time

2 days ago
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Job summary

Bausch + Lomb in Waterford, Ireland, is seeking a QA Shift Lead to ensure quality across manufacturing processes on the floor. You will partner with Operations, Maintenance, and QA to contain non-conforming product, perform audits, and drive continuous improvement.

The role requires strong GMP knowledge, documentation control, and the ability to lead investigations and CAPAs. Experience in pharma/medical device environments is preferred; on-site work in Waterford.

Qualifications

  • Experience in a medical-device or pharmaceutical environment.
  • Strong numerical and data analysis abilities.
  • Familiarity with GMP and quality systems.
  • Excellent verbal and written communication.
  • Ability to work autonomously on quality investigations.
  • Proficient with MS Office; ECDL desirable.

Responsibilities

  • Coordinate containment of non-conforming product and material.
  • Assist with disposition decisions on the manufacturing floor.
  • Lead shift-by-shift quality decisions and investigations.
  • Initiate and process NCRs.
  • Perform data analysis and trend monitoring.
  • Support complaint handling and investigations.
  • Review records independently.
  • Support process improvement and CAPA initiation.
  • Ensure SOPs followed and GMP requirements met.
  • Maintain clean, compliant work area.

Skills

cGMP knowledge
Documentation control
Quality systems
Analytical skills
Detail-oriented
Communication
DB management
MS Office
Documentum
CAMS/CATSweb
Pharma experience

Tools

Documentum
CAMS/CATSweb

Job description

Bausch + Lomb in Waterford, Ireland, is seeking a QA Shift Lead to ensure quality across manufacturing processes on the floor. You will partner with Operations, Maintenance, and QA to contain non-conforming product, perform audits, and drive continuous improvement.

The role requires strong GMP knowledge, documentation control, and the ability to lead investigations and CAPAs. Experience in pharma/medical device environments is preferred; on-site work in Waterford.

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