Based in Roscommon with a MedTech company, the successful candidate will be responsible for supporting company operation activities and be accountable for manufacturing activities at each stage of manufacturing.
This position will be offering a permanent contract working days only
Assisting with planning and tracking of production batches through full manufacturing process.
Assists Quality and Production personnel in identifying and correcting non-conformances. Communicates with production personnel, warehouse, engineering, and management regarding inspection results and corrective actions
Completes appropriate manufacturing documentation (e.g. BMR), including Inspection records.
Notifies production personnel of non-conformances observed.
Follows safety policies and quality system requirements.
Actively develops and participates in any and all reasonable work activities and projects as may be deemed suitable and assigned by management.
Works towards the identification and reduction of non-value activities
Conforms to, supports, and enforces all Company policies and procedures.
Previous experience in a manufacturing environment is desirable.
Decision making ability coupled with the ability to work on ones’ own initiative and with minimum supervision is required.
Ability to communicate (written and oral) and work with people inside and outside the department.
Ability to co-ordinate, plan and organise
Rigorous attention to detail and a methodical work discipline are essential prerequisites for the successful candidate to ensure effective implementation and monitoring of quality processes, controls and procedures.
For a confidential discussion and more information on the role, please contact Eoghan Dalton.