Manufacturing Technician

Our Client, A leading Medical Device company based in Clare, are seeking a Manufacturing Technician to join their team. The Manufacturing Technician will manufacture products in compliance with all quality and safety requirements, provide manufacturing support to process & product development, support process improvements, and support validation activities within the company. 

Responsibilities include but are not limited to:

• Manufacture of products both onsite and at subcontractors/suppliers to ensure that the product quality, regulatory & business requirements are met.
• Provide Manufacturing support to R&D to develop and improve process and product development projects.
• Creation, update and review of documentation including Batch records, procedures etc.,
• Ensure all items of equipment are maintained following the maintenance and calibration procedures and schedules.
• Ensure all health, safety and environmental requirements are met.
• Track and report progress across projects by reviewing schedules and due dates, identifying risks and implementing contingency plans.
• Support the Quality Management System through resolution of NCR, NCM's and CAPAs ensuring effective solutions are implemented.
• Stock and inventory management using the ERP system.
• Support Validation Activities including execution of protocols for equipment and process validations.
• Review and contribute to supplier process validation and risk management activities.
• Introduce, Assess and approve process changes ensuring product impact is appropriately considered.
• Provide support during internal and external audits.
• Compile any necessary equipment/capital authorization requests supported with appropriate justifications and alternative options.
• Carry out process and safety risk assessments, and pFMEAs.
• Communicate effectively with all Internal & External Stakeholders.
• Collaborate with key suppliers and their production/manufacturing teams to drive and support process/product improvements/developments.

• Minimum 2 years industry experience in GMP regulated environment.
• Relevant Level 7/8 qualification in Science/Engineering
• Previous experience with Bio Materials would be advantageous 
• Experience working in a Good Manufacturing Practices environment
• Good planning and organizational skills.
• Excellent communication, interpersonal and presentation skills.
• Ability to work both independently and as part of a team.
• Ability to manage multiple projects and prioritize workload effectively to meet project deadlines.
• Ability to work both independently and as part of a team

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other or future related vacancies.

Pale Blue Dot® Recruitment - The Resource for the MedTech Workforce