Thermo Fisher Scientific
Operations Training Specialist - First Shift
LMS
Edtech.com's Summary
Thermo Fisher Scientific is hiring an Operations Training Specialist to develop and maintain training programs for manufacturing operations in a GMP environment. The role involves coordinating training initiatives, creating engaging content, ensuring regulatory compliance, and collaborating with cross-functional teams to support continuous learning and operational excellence.
Highlights
- Develop and deliver training programs for pharmaceutical manufacturing operations.
- Manage comprehensive training initiatives and maintain documentation systems.
- Ensure compliance with cGMP regulations and support regulatory audits.
- Utilize Learning Management Systems (LMS), e-learning platforms, and Microsoft Office tools.
- Require 4 years of GMP manufacturing experience, preferably in pharmaceutical or clinical operations.
- Preferred formal training qualification or certification and strong presentation skills.
- Work includes cleanroom requirements and adherence to safety standards.
- Strong organizational, project management, and communication skills are necessary.
- Collaborate across departments to identify training needs and improve processes.
- Flexibility to work various shifts and ability to lift 40 lbs. without assistance.
Operations Training Specialist - First Shift Full Description
Operations Training Specialist - First Shift
Location Lebanon, Tennessee, United States of America
Operations
Remote Fully Onsite
Operations
Remote Fully Onsite
Work Schedule
First Shift (Days)
First Shift (Days)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION: We are seeking a Operations Training Specialist at Thermo Fisher Scientific, where you will have a key role in developing and maintaining comprehensive training programs for our manufacturing operations. You will ensure employees are equipped with the knowledge and skills needed to maintain our high standards of quality and compliance in pharmaceutical manufacturing. Working in a GMP environment, you will coordinate comprehensive training initiatives, develop engaging content, and support a culture of continuous learning and excellence. Your contributions will enhance the organization as you design and implement training programs, maintain documentation systems, and ensure regulatory compliance. You will collaborate with cross-functional teams to identify training needs, create effective learning solutions, and track program effectiveness. This role contributes directly to our mission of enabling our customers to make the world healthier, cleaner, and safer.
REQUIREMENTS: • 4 years of experience in GMP manufacturing environment, preferably in pharmaceutical or clinical operations • Preferred Fields of Study: Education, Training, or relevant discipline • Formal training qualification or certification preferred • Strong knowledge of cGMP regulations and good documentation practices • Experience developing and delivering training programs and materials • Proficiency in Learning Management Systems (LMS) and training documentation systems • Advanced skills in Microsoft Office Suite, particularly PowerPoint and Excel • Experience with e-learning platforms and digital training tools • Strong presentation and facilitation abilities • Excellent organizational and project management skills • Superior written and verbal communication skills • Ability to work independently and manage multiple priorities • Experience supporting regulatory audits and inspections • Demonstrated ability to collaborate effectively across departments • Strong attention to detail and accuracy in documentation • Flexibility to work various shifts as needed • Ability to work in cleanroom environments and follow GMP requirements • Problem-solving skills and ability to recommend process improvements
REQUIREMENTS: • 4 years of experience in GMP manufacturing environment, preferably in pharmaceutical or clinical operations • Preferred Fields of Study: Education, Training, or relevant discipline • Formal training qualification or certification preferred • Strong knowledge of cGMP regulations and good documentation practices • Experience developing and delivering training programs and materials • Proficiency in Learning Management Systems (LMS) and training documentation systems • Advanced skills in Microsoft Office Suite, particularly PowerPoint and Excel • Experience with e-learning platforms and digital training tools • Strong presentation and facilitation abilities • Excellent organizational and project management skills • Superior written and verbal communication skills • Ability to work independently and manage multiple priorities • Experience supporting regulatory audits and inspections • Demonstrated ability to collaborate effectively across departments • Strong attention to detail and accuracy in documentation • Flexibility to work various shifts as needed • Ability to work in cleanroom environments and follow GMP requirements • Problem-solving skills and ability to recommend process improvements
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