Job Requirements:
- 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.
- Measure and report RFT / trend data and work with departments to resolve recurring issues.
- Participate in internal supplier and regulatory audits and key quality initiatives as appropriate.
- Perform critical/ constructive review of procedures and practices.
- Support investigation of deviations ensuring all product deviations are closed prior to product release.
- Ensure compliance to cGMP at all times.

Qualifications & Experience:
- 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.
- Good presentation skills.
- Working knowledge of computer packages.
- Flexible approach – comfortable with on-going change.

Personal Characteristics:
- Takes personable responsibility for their actions.
- Excellent attention to detail.
- Good communicator who is comfortable to work as part of a team.
- Focused on achieving results.
- Self-starter and able to work under minimum supervision.