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Manufacturing Training Coordinator
Career Insights for Technical Trainer
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Scorecard
Based on Georgia data
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What they do
A Technical Trainer is responsible for designing and leading technical training programs for staff at an organization or company. Works with the employees to determine their technical requirements and therefore their training needs and objectives; provides presentations, workshops or technology-supported training.
$64,308 / year median in Georgia
+1% projected growth
Job Description
Manufacturing Training Coordinator Union Agener - 3.0 Augusta, GA Job Details 3 days ago Benefits Employee assistance program 401(k) matching Qualifications Incident investigation techniques for hazard identification Program design Content creation for technical audiences Defect resolution root cause analysis Technical documentation Coaching Technical writing experience within manufacturing Manufacturing standard operating procedures Manufacturing facility experience Corporate training program coordination Pharmaceutical company experience Mentoring Instructor-led training (training delivery method) Project management methodology Investigative reports Productivity software Incident report writing Chemical plant experience Standard operating procedures (SOPs) Technical Proficiency Cross-functional communication Standard operating procedures drafting Data analysis software Failure analysis Pharmaceutical manufacturing facility experience
Full Job Description Position Description, Functions, Duties and Tasks:
Position Summary:
The Manufacturing Training Coordinator plays a critical role in ensuring operational training excellence, safety, and regulatory compliance across the manufacturing facility. Reporting directly to the API or Drug Product Manager, this position leads the design, standardization, and execution of site and area training programs, provides training guidance to the area SME Trainers, drives Continuous Improvement (CI) initiatives, and acts as a lead technical writer for training materials. The ideal candidate is a high-energy, self-directed problem solver with a strong background in training program development and management in a regulated chemical, pharmaceutical, or process manufacturing environment.
Responsibilities:
Training Standard Operating Procedures (SOPs): Create, update (practice vs procedure) and distribute procedures/modules/JFC's to manufacturing personnel.
Employee Onboarding and Training :
Onboard new operations personnel, conduct needs assessments via SME input and workplace observations, and execute hands-on competency validations. Complete routine check-ins.
Communication:
Maintain effective communication with the Operations/Manufacturing managers, shift leaders and support staff to ensure adherence to protocols and standards
Team Collaboration:
Actively participate in area team meetings and project teams.
Qualification Plans:
Develop and facilitate employee qualification plans and partner with production leaders to ensure employees remain in qualified status.
Train-the-Trainer Programs:
Facilitate Train-the-Trainer certification programs to empower Supervisors and Subject Matter Expert Trainers (SMETs) to deliver consistent, high-quality training.
Continuous Improvement Performance Gap Identification:
Monitor shop-floor operations and evaluate training data to identify skill deficiencies, operational bottlenecks, and efficiency opportunities.
Quality & Work Standardization:
Develop and implement department-wide quality control measures and standardized work routines to minimize variance.
Project Implementation:
Act as a champion for Continuous Improvement (CI) initiatives, new operational tools, and site-wide process optimizations.
Operational Support:
Assist Operations Managers in planning, developing, and coordinating plant-wide activities to minimize operational disruptions.
Deviation Investigator/Quality Compliance Technical Writing Support:
Provide technical writing support for non-routine investigations rooting in human error or training inadaquacies.
Deviation Management:
Support the operational implementation of deviation-specific countermeasures. Minimum Qualification (Education, Experience and/or Training, Required Certifications):
Education:
Associate Degree in Engineering, Technical Science, or a related discipline (or equivalent relavent experience).
Experience:
Minimum of 3-5 years of experience in a chemical, pharmaceutical, or regulated process manufacturing environment.
Core Experience:
Proven track record in developing, delivering, and evaluating workforce training programs. Proven proficiency in manufacturing processes and equipment is required. The successful candidate must be capable of serving as a subject matter expert, providing training, mentorship, and technical guidance to trainees and team members.
Skills:
Technical Writing:
Superior ability to translate complex manufacturing processes into clear SOPs, SWIs, technical investigation reports, and training guides.
Software & Systems Proficiency:
Proficiency in ERP systems (SAP preferred), Quality Management Systems (e.g., SESuite), MS Office Suite (Word, Excel, PowerPoint, Teams), and Adobe.
Methodology Expertise:
Knowledge of Job Instruction Training (JIT), Standard Work Instructions (SWIs), Root Cause Analysis (RCA) techniques and TAP Root.
Interpersonal & Coaching:
Strong public speaking, facilitation, and coaching abilities to engage cross-functional teams and manufacturing associates.
Additional Preferences:
Manufacturing background Additional technical training Knowledge of API/Drug Product process areas and cGMPs Familiarity with DCS and PLC automation systems Familiarilty with data historian Experience as a deviation investigator and CAPA management. Green Belt Certification or CI Certification What do we offer? Competitive Salary Competitive Benefits Package and Employee Assistance Program 401(k) Plan
+ Company Match Vacation
+ End of Year Vacation (Company Sponsored) Growth Opportunities to expand your career
Benefits
- Health and Wellness Programs
- 401(k) Plans
- Dental Insurance