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Open nowPosted today

Operations Training Specialist III

thermofisher2,754 open roles

Where
Greenville, North Carolina, USA
Work mode
On site
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Your applicationOpen nowOperations Training Specialist IIIthermofisher · Greenville, North Carolina, USA

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. thermofisher postings stay open a median of 10 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted today

thermofisher median: 10 days open

The posting

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance

Job Description

Job Title: Operations Training Specialist III

Location: Greenville, NC

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.

Location/Division Specific Information

Greenville, NC

As part of the Drug Product Division (DPD), our Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus supporting sterile injectable and oral solid dose drug products from development through commercialization.

This position supports sterile pharmaceutical manufacturing within our Quality Assurance Training and Development team. Working closely with Manufacturing, Quality, Engineering, and other technical partners, you'll help develop employee capabilities, strengthen operational performance, and support regulatory compliance.

How will you make an impact?

As an Operations Training Specialist III, you'll combine hands-on instruction with innovative training development to help employees build the knowledge, skills, and confidence needed to succeed in a regulated pharmaceutical manufacturing environment.

This role offers a balanced mix of instructor-led training (approximately 50%) and instructional design and development (approximately 50%).

You'll participate in our structured new employee training program while developing learning solutions for new manufacturing processes, equipment, and technologies. Working directly with subject matter experts and operational teams, you'll translate complex technical information into engaging, practical learning experiences.

This is an excellent opportunity for an experienced training professional or a manufacturing specialist with a passion for teaching to expand their instructional design capabilities while making a meaningful impact on employee development and operational excellence.

What will you do?

  • Deliver engaging instructor-led training as part of a structured four-week onboarding program covering approximately 30 operational courses.
  • Develop proficiency across the training curriculum and facilitate classroom, hands-on, and individualized learning experiences.
  • Design and develop training materials for manufacturing processes, equipment, technologies, and operational procedures.
  • Partner with subject matter experts, Manufacturing, Engineering, Validation, and Quality to translate technical information into effective learning solutions.
  • Create interactive training content, including eLearning, videos, presentations, simulations, practical exercises, and proficiency assessments.
  • Evaluate training effectiveness, provide coaching and targeted retraining, and continuously improve learning outcomes.
  • Coordinate training development projects, managing stakeholders, priorities, timelines, and deliverables.
  • Maintain accurate training documentation and ensure alignment with cGMP requirements, quality systems, and established procedures.

Education

  • Bachelor's degree in Education, Instructional Design, Business, Life Sciences, Engineering, or a related field is preferred.
  • Associate degree with relevant manufacturing, training, or operational experience may be considered.
  • Candidates without a college degree who demonstrate substantial relevant experience and strong instructional capabilities may also be considered, subject to applicable job qualification requirements.

Experience

Experience in training, learning and development, instructional design, pharmaceutical manufacturing, sterile operations, or another regulated manufacturing environment is preferred.

Candidates with hands-on manufacturing experience who have trained, coached, or qualified colleagues are encouraged to apply. Formal classroom instruction experience is beneficial but not required for individuals who demonstrate strong communication skills and the ability to develop effective learning materials.

The ideal candidate brings a combination of practical operational knowledge, instructional ability, and an interest in developing others.

Knowledge, Skills and Abilities

  • Strong understanding of adult learning principles and the ability to deliver engaging, effective instruction.
  • Excellent analytical, problem-solving, communication, and interpersonal skills.
  • Knowledge of aseptic gowning practices within sterile or controlled manufacturing environments.
  • Ability to translate technical information into clear training materials, practical exercises, and learner assessments.
  • Proficiency with Microsoft Office and the ability to develop computer-based learning materials.
  • Strong organizational and project coordination skills, with the ability to manage multiple priorities independently and collaboratively.
  • Ability to engage effectively with manufacturing employees, technical experts, and cross-functional stakeholders.
  • Familiarity with cGMP requirements, quality systems, and regulated manufacturing practices is preferred.
  • Experience with instructional design tools such as Articulate, Adobe Creative Cloud, Captivate, or similar platforms is preferred.
  • Experience with eLearning, multimedia development, learning management systems, or immersive learning technologies is a plus.

Physical Requirements / Work Environment

This is an on-site position based at our Greenville, North Carolina pharmaceutical manufacturing facility.

The role involves classroom instruction, computer-based training development, collaboration with operational teams, and periodic visits to manufacturing areas. Employees must follow applicable safety, gowning, and site access requirements when entering controlled environments.

The position requires the ability to stand during training sessions, move throughout the facility, and operate computers and audiovisual equipment.

Routine business travel is not anticipated.

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