Operations Training Specialist

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION: We are seeking an 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.

Education& Experience:

• High school diploma or equivalent.

• PreferredExperience:Previouswork experience ina cGMP environmentmanufacturing operations productionorwarehouse.

3 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

What We Offer:

Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities