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Training Lead

Location Covingham, Swindon, Wiltshire, United Kingdom Job Id R-01309795 Job Type Full time Category Quality & Regulatory Remote Fully Onsite
The Quality Difference at Thermo Fisher Scientific: What makes our quality teams unique is a shared passion for getting it done right the first time and working for the right reasons with our customers always in mind. Our team of Quality professionals understand our customers rely on the accuracy, safety, and effectiveness of our products and services that are improving lives around the world. When you join our team of quality professionals, you’ll collaborate on projects on a global scale while being encouraged to grow your skills and discover new career paths with us.
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, ashering 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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"Quality is everyone's responsibility. Right the first time should not be only a metric, but a lifestyle."


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