**Job Title:** Manufacturing Technician
CREGG is currently recruiting a skilled Manufacturing Technician for a leading Medical device and Pharmaceuticals company in Shannon, Co. Clare.
We are seeking an experienced professional to join our team and contribute to the development of various exciting projects. This role offers not only opportunities for career growth but also the chance to make a significant impact in the medical device industry.
Summary
* Manufacture products in compliance with all quality and safety requirements.
* Provide manufacturing support to process & product development.
* Support process improvements.
* Assist with validation activities.
This role plays a vital part in ensuring product quality, regulatory compliance, and business needs during manufacturing, including at subcontractors/suppliers. Additionally, you will provide support to R&D for process and product development, while managing and updating necessary documentation.
Key Responsibilities
1. Ensure product quality, regulatory compliance, and business needs during manufacturing, including at subcontractors/suppliers.
2. Provide support to R&D for process and product development, while managing and updating necessary documentation (e.g., Batch records, procedures).
3. Maintain equipment and ensure health, safety, and environmental compliance, tracking project progress and addressing risks.
4. Support the Quality Management System by resolving NCR, NCMs, and CAPAs, and manage stock/inventory using ERP systems.
5. Assist with validation activities, process changes, and risk management, collaborating with suppliers to enhance production processes.
6. Support audits, conduct risk assessments, and submit capital authorization requests with appropriate justifications.
We require a dedicated individual with excellent planning, organizational, communication, interpersonal, and presentation skills. You should be able to work both independently and as part of a team, with the ability to manage multiple projects and prioritize workload effectively to meet project deadlines.
The ideal candidate will have a minimum of 6 months' industry experience in a GMP regulated environment or hold a relevant level 7/8 qualification in Science/Engineering. Graduates with a level 8 in Biomedical science or a related field will also be considered.
We offer a competitive salary, along with benefits including:
* Paid holidays.
* Parking.
* Pension.
* Educational assistance.
* Compressed hours.
* Life Assurance.
* Permanent Health Insurance.