3rd Shift Finishing Trainer - GMP Training & Onboarding

Grand River Aseptic Manufacturing, Inc.; Grand Rapids (MI); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Benefits starting day 1

Paid volunteerism starting day 1

PTO: 13 days/year

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing, Inc. is seeking a Training Specialist to onboard new hires and deliver job-specific training.

You will coordinate with the training coordinator and area supervisors to ensure procedures and cGMP regulations are followed, and you will support finishing area tasks as needed. The role emphasizes on-the-job, instructor-led, and read/understand trainings, plus handling Good Documentation Practices and training Master Control usage.

Qualifications

• 1+ years in an FDA regulated environment or a college degree equivalent.
• Knowledge of QA principles in pharma/biopharma/biotech manufacturing.
• Experience in pharmaceutical packaging with understanding of cGMP, FDA guidelines and multinational standards.
• Knowledge of GMP standards and CFR guidelines.
• Detail oriented.
• Proficient with Word, Excel, Outlook.

Responsibilities

• Follow/train all labeling, packaging, and finishing procedures.
• Assist/train in equipment setup and operation.
• Accurately perform/train Good Documentation Practices.
• Assist/train in completion of batch record materials.
• Assist with training of Master Control and its general use.
• Track/verify that all individuals have completed necessary training courses.
• Actively engage/train current Good Manufacturing Practices.
• Train new hires as well as veteran employees.
• Actively participate in Continuous Quality and Safety Improvements.

Skills

Detail oriented

Training / coaching

Documentation skills

Education

Bachelor's degree or equivalent

Tools

Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing, Inc. is seeking a Training Specialist to onboard new hires and deliver job-specific training.

You will coordinate with the training coordinator and area supervisors to ensure procedures and cGMP regulations are followed, and you will support finishing area tasks as needed. The role emphasizes on-the-job, instructor-led, and read/understand trainings, plus handling Good Documentation Practices and training Master Control usage.