QA Operations Specialist — Drive GMP Excellence

Sanofi; Munster; On-site; EUR 42,000 - 62,000; Full time

Job summary

Sanofi Waterford in Ireland is seeking a Quality Assurance Specialist to join our GMP-compliant QA team. Based in Waterford, you will review documentation, support investigations, and ensure timely closure of quality actions while promoting continuous improvement.

The role requires a science degree, at least 2 years in a GMP environment, excellent attention to detail, strong interpersonal skills, and proficiency with common computer packages.

Qualifications

• Third level qualification (degree in science or related discipline preferred).
• Minimum of 2 years' experience in a similar role.
• Experience working in a GMP environment is required.
• Very good knowledge of cGMP in a regulated environment.
• Excellent accuracy and attention to detail.
• Excellent interpersonal skills.
• Flexible approach – comfortable with ongoing change.
• Good presentation skills.
• Working knowledge of computer packages.

Responsibilities

• Acts as Quality Point person for systems / processes providing guidance / feedback on quality issues.
• Perform timely review of documentation / investigations / reports highlighting and assisting in the resolution of concerns commensurate with the risk.
• Work with relevant departments to ensure timely closure of quality actions / findings.
• Actively contribute to continuous improvement initiatives.
• Conduct duties in a safe manner and report all safety issues or concerns.
• Maintain work area to good housekeeping standards.
• Ensure attendance at place of work when required.
• Support team in achieving team goals/targets.
• Attend team meetings as required.
• Actively contribute to continuous improvement initiatives.

Skills

Quality Assurance

GMP experience

Attention to detail

Communication skills

Education

Science degree

Tools

Microsoft Office

Job description

Sanofi Waterford in Ireland is seeking a Quality Assurance Specialist to join our GMP-compliant QA team. Based in Waterford, you will review documentation, support investigations, and ensure timely closure of quality actions while promoting continuous improvement.

The role requires a science degree, at least 2 years in a GMP environment, excellent attention to detail, strong interpersonal skills, and proficiency with common computer packages.