Incoming QA Lead – Life Sciences Diagnostics

Radiometer; Maryfort or Lismeehan; Presencial; EUR 70 000 - 90 000; Tempo integral

Resumo da oferta

Beckman Coulter Diagnostics in Ireland is seeking a Supervisor - Quality Assurance to lead the incoming inspection team and ensure timely release of materials. You will support GMP compliance, training, and cross-functional collaboration to uphold quality across operations.

Ideal candidates hold a BSc/MSc in a relevant field with 3+ years in an FDA-regulated setting, strong communication, and meticulous attention to detail. This on-site role sits in Co.

Qualificações

• BSc or MSc in Chemistry, Biochemistry, Microbiology, Engineering, or a related field with at least 3 years’ FDA-regulated industry experience.
• Excellent time management and organisation skills and ability to work on own initiative.
• Effective interpersonal and verbal/written communication skills.
• Strong proofreading skills with emphasis on attention to detail.

Responsabilidades

• Ensure all Incoming Inspection activities are completed with accuracy and compliance.
• Participate in cross-functional teams, providing Incoming Inspection support to all departments, ensuring GMP and Quality System Regulations are followed during ordering and receipt.
• Prioritise and address supplier quality issues identified through receiving or incoming inspection, especially NC/SCAR.
• Manage, communicate with, and develop area personnel, including training inspectors on procedures, cGMPs, and documentation control.
• Generate, analyse, and report quality metrics to drive ongoing improvement programs.

Conhecimentos

Time management

Organization

Communication

Proofreading

Formação académica

BSc or MSc in Chemistry/Biochemistry/Microbiology/Engineering

Descrição da oferta de emprego

Beckman Coulter Diagnostics in Ireland is seeking a Supervisor - Quality Assurance to lead the incoming inspection team and ensure timely release of materials. You will support GMP compliance, training, and cross-functional collaboration to uphold quality across operations.

Ideal candidates hold a BSc/MSc in a relevant field with 3+ years in an FDA-regulated setting, strong communication, and meticulous attention to detail. This on-site role sits in Co.