TE Connectivity logo

ADMINISTRATIVE SUPPORT V/TRAINING SPECIALIST

TE Connectivity
Department:Manufacturing
Type:ON-SITE
Region:Galway
Location:Galway, County Galway, Ireland
Experience:Associate
Estimated Salary:€35,000 - €50,000
Skills:
TRAINING MATERIAL CREATIONTRAINING DELIVERYREGULATORY COMPLIANCEISO 13485MDSAPMS WORDEXCELPOWERPOINTQUALITY MANAGEMENTMEDICAL DEVICES
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Job Description

Posted on: August 23, 2025

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview Reporting to the Quality Systems Supervisor, the training Specialist in the Training Department, you will play a crucial role in ensuring the effectiveness and compliance of our training programs for employees in TE connectivity. Training Specialist will work closely with cross-functional teams to develop, implement, and evaluate training materials and procedures, while also supporting continuous improvement initiatives to enhance our quality management system. Job Requirements

  • Support day-to-day activities in the training department.
  • Provide guidance the team in support of the day-to-day deliverables.
  • Own Investigation of root cause and implementation of effective actions to prevent re-occurrence of compliance issues.
  • Training Material Creation: Create and maintain training materials to support effective learning outcomes.
  • Training Delivery: Facilitate training sessions for employees including induction training, ensuring content is delivered clearly and comprehensively, and providing guidance and support as needed.
  • Training Evaluation: Evaluate the effectiveness of training through assessments review, and performance metrics, and make recommendations for improvement.
  • Regulatory Compliance: Stay abreast of regulatory requirements and industry best practices related to training and quality management and ensure training programs are compliant with relevant standards (e.g., ISO 13485, MDSAP requirements…).
  • Cross-Functional Collaboration: Collaborate with various departments, including Quality Operations, Manufacturing, and Human Resources, to integrate training initiatives into overall quality and compliance strategies.
  • Continuous Improvement: Identify opportunities for process improvements within the training department and contribute to initiatives aimed at enhancing the efficiency and effectiveness of training programs.
  • Support Audits and own actions for CAPA, NC’s, Audit findings.
  • Other tasks as directed by the Senior Quality Systems Engineer in line with company goals and objectives

Key Requirements

  • Excellent communication and presentation skills, with the ability to convey complex information clearly and effectively.
  • Detail-oriented mindset with analytical and problem-solving abilities.
  • Ability to work collaboratively in a cross-functional team environment.
  • Flexible highly motivated individual with the ability to work on their own initiative.
  • Pro-active, practical and innovative approach to everyday activities.
  • Good working knowledge of regulatory requirements and audits.
  • Background and experience in medical devices would be an advantage.
  • Computer literate, MS Word, Excel, PowerPoint.

What your background should look like

  • Level 7 degree in Science / Engineering / Quality Management or related fields essential or equivalent industry experience .
  • Minimum of 2 years’ industry experience in a Medical devices manufacturing environment.
  • Experience within training or Quality systems department is desirable.

Competencies Values: Integrity, Accountability, Inclusion, Innovation, Teamwork

Originally posted on LinkedIn

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