QA Supervisor – Incoming Inspection (Life Sciences)

Beckman Coulter Diagnostics; Munster; On-site; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Benefits program

Job summary

Beckman Coulter Diagnostics, a Danaher operating company, seeks a Supervisor - Quality Assurance to manage the incoming inspection team on-site in Co. Clare. You will ensure GMP/compliance and timely release of materials to operations.

You will lead cross-functional teams, train inspectors on procedures and cGMPs, and drive quality metrics for continual improvement within the Operations Quality dept.

A BSc/MSc in a technical field and 3+ years in an FDA-regulated industry are required.

Qualifications

• 3 years’ experience in an FDA‑regulated industry.
• Excellent time management and organisation skills.
• Effective interpersonal and verbal/written communication skills.
• Strong proofreading skills with emphasis on attention to detail.

Responsibilities

• 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 complied with during the ordering and receipt of product.
• Ensure supplier‑related quality issues identified through the receiving or incoming inspection process are effectively prioritised and acted upon in a timely manner, particularly those in the NC / SCAR process.
• Management of, communication with, and development of area personnel, including training inspectors on procedures, cGMPs, and documentation control
• Generate, analyse, and report quality metrics to relevant personnel to ensure ongoing improvement programs are put in place.

Skills

Time management

Organization

Communication

Proofreading

Education

BSc/MSc in Chemistry

Tools

Lean methodologies

Job description

Beckman Coulter Diagnostics, a Danaher operating company, seeks a Supervisor - Quality Assurance to manage the incoming inspection team on-site in Co. Clare. You will ensure GMP/compliance and timely release of materials to operations.

You will lead cross-functional teams, train inspectors on procedures and cGMPs, and drive quality metrics for continual improvement within the Operations Quality dept.

A BSc/MSc in a technical field and 3+ years in an FDA-regulated industry are required.