Skip to content

Manufacturing Technician

  • On-site
    • Clare, Munster, Ireland
  • Engineering ( Production/Process Dev/Manufacturing)

Job description

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.

Job requirements

  • 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

or

Apply with Linkedin unavailable
Apply with Indeed unavailable