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Training Lead

Thermo Fisher Scientific

Swindon

On-site

GBP 60,000 - 80,000

2 days ago
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Job summary

An established industry player is seeking a dynamic Training Lead to enhance workforce capabilities in compliance with cGMP standards. This role involves crafting and implementing effective training programs, fostering a culture of continuous learning, and ensuring adherence to regulatory requirements. As a Subject Matter Expert, you will leverage your creativity and excellent communication skills to deliver impactful training initiatives. Join a team that values innovation and dedication, where your contributions will directly influence the success of the workforce and the organization as a whole. If you are passionate about training and development, this opportunity is perfect for you.

Qualifications

  • CIPD qualified with experience in specialist training in manufacturing.
  • Excellent communication and presentation skills are essential.

Responsibilities

  • Develop and implement sustainable cGMP training programs.
  • Coordinate site-wide training delivery and monitor compliance metrics.

Skills

Training Development

Communication Skills

Creativity

Time Management

Interpersonal Skills

Education

CIPD Qualification

Experience in Pharmaceutical Industry

Tools

Success Factors Learning Management System

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Position Summary:

Join Thermo Fisher Scientific Inc. as a Training Lead in Swindon, UK, develop and implement sustainable cGMP training to ensure a well-trained workforce and in compliance with all regulations.

Responsibilities:

  • Own and craft the health of training at the site.
  • Develop detailed training programs and implement in partnership with Department Managers and Specialists.
  • Build and deliver value-adding training aligned with organisational goals, adhering to GMP requirements and company policies.
  • Serve as the Subject Matter Expert for the Success Factors Learning Management System, improving training efficiencies.
  • Conduct gap analyses of Authority regulations, global documents, and audit observations, and adjust training programs accordingly.
  • Coordinate and support site-wide training administrators to ensure cohesive training delivery and recording.
  • Develop measurement criteria to assess the efficiency of training and monitor compliance metrics, reporting key learning metrics to site leadership.
  • Facilitate site onboarding programs and support apprenticeships and intern placements.
  • Provide specialist training support during Regulatory Inspections.
  • Champion Global training initiatives at a site level.
  • Implement a standardised competence-based program for department trainers.
  • Deputise for the Quality Systems & Compliance Manager when needed.

Minimum Requirements/Qualifications:

  • CIPD qualified or similar, with experience in rolling out specialist training activities in a manufacturing setting. Pharmaceutical experience is advantageous.
  • Dynamic proactive approach to tackling meaningful assignments.
  • Creativity and excellent presentational skills.
  • Ability to work within critical timelines.
  • Excellent interpersonal, oral, and written communication skills.
  • A high degree of self-motivation and independence.
  • A passion to set people up for success in their roles!
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