Finishing Training Specialist - Pharma & GMP

Grand River Aseptic Manufacturing Inc.

Grand Rapids, Northern (MI, KY)

Hybrid

USD 45,000 - 65,000

Full time

13 days ago
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Benefits offered by this job

Benefits starting day 1
Paid volunteerism 16 hours/yr
PTO 13 days/yr
Wellness time off
Paid holidays 10 per year

Job summary

Grand River Aseptic Manufacturing Inc. is seeking an onboarding trainer to facilitate training for new hire trainees in a FDA-regulated, cGMP environment.

Coordinate with the training coordinator and area supervisors to meet established procedures and cGMP guidelines, and support on-the-job and instructor-led trainings in finishing areas. Responsibilities include training in labeling, packaging, equipment setup, and Good Documentation Practices; track completion of courses and train both new

Qualifications

  • Experience in FDA regulated/pharma manufacturing environment preferred.
  • Knowledge of QA principles and CFR/good manufacturing practices guidelines.
  • Experience with pharmaceutical packaging and CFR guidelines.
  • Detail oriented with strong documentation skills.
  • Proficient in Word, Excel, and Outlook.

Responsibilities

  • Follow/train 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 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

FDA regulated experience
QA principles
GMP knowledge
Detail oriented
MS Office (Word, Excel, Outlook)

Education

College degree or equivalent

Tools

Microsoft Office

Job description

Grand River Aseptic Manufacturing Inc. is seeking an onboarding trainer to facilitate training for new hire trainees in a FDA-regulated, cGMP environment.

Coordinate with the training coordinator and area supervisors to meet established procedures and cGMP guidelines, and support on-the-job and instructor-led trainings in finishing areas. Responsibilities include training in labeling, packaging, equipment setup, and Good Documentation Practices; track completion of courses and train both new

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