Impactful 3rd-Shift Finishing Trainer | Pharma GMP

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Benefits starting day 1 (medical, etc)

Paid volunteerism 16 hours/year

PTO 13 days/year

Wellness time off

10 paid holidays

Job summary

Grand River Aseptic Manufacturing (GRAM) seeks a Training Specialist to facilitate onboarding and provide job-specific training in a cGMP, FDA-regulated environment. You will coordinate with training coordinators and area supervisors to ensure adherence to procedures and regulatory standards, and support finishing area tasks as needed.

Responsibilities include training in labeling, packaging, setup, and Good Documentation Practices, with emphasis on thoroughness and process improvement.

Qualifications

• 1+ years relevant experience in FDA regulated environment or college degree equivalent.
• Knowledge of QA principles in pharma, biopharma, and/or biotech manufacturing.
• Experience in pharmaceutical packaging with understanding of cGMP, FDA guidelines and multinational regulatory standards.
• Knowledge of GMP standards and CFR guidelines.
• Must be detail oriented.
• Proficient in Word, Excel, and 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

FDA regulated environment experience

QA principles

cGMP knowledge

Detail oriented

Education

Bachelor's degree or equivalent

Tools

Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) seeks a Training Specialist to facilitate onboarding and provide job-specific training in a cGMP, FDA-regulated environment. You will coordinate with training coordinators and area supervisors to ensure adherence to procedures and regulatory standards, and support finishing area tasks as needed.

Responsibilities include training in labeling, packaging, setup, and Good Documentation Practices, with emphasis on thoroughness and process improvement.