Role and Responsibilities

• Ensure the effective implementation and maintenance of the Quality Management System.
• Perform QA Verification of activities performed in intake, manufacture & distribution.
• Support the operation of QMS functions, such as:
• Change Controls, CAPAs and Non-Conformance documentation, documentation control, Employee Training, design & development controls.
• Support continuous improvement initiatives based on quality objectives.
• Participate in Notified Body Audits and Audit preparation as requested.
• Generate reports as required and assist in any other data compilation as requested.
• Assist in other projects as required.

Qualifications and Education Requirements

• Qualifications: Third level qualification in natural sciences (Certificate, Diploma, Degree level)
• Good planning and organizational skills.
• 2+ years’ experience in a highly regulated industry (Pharma, food, medical devices).
• Good communication skills (oral and written).
• Hardworking and highly motivating individual, with good attention to detail.
• Proficient in use of Microsoft Office.
• Ability to work both independently and as part of a team.
• Ability to work in a dynamic environment, with changing priorities.

Note: This description reflects essential functions and does not prescribe nor restrict tasks that may be assigned.