QA Finishing Ops Specialist, Pharma Quality & Impact

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Benefits starting day 1

Paid volunteer time

PTO 13 days/year

Wellness time off

Paid holidays

Pay: depends on experience

Job summary

Grand River Aseptic Manufacturing (GRAM) is seeking a QA Specialist I in Finishing Operations to support cGMP quality systems for terminal sterilization, visual inspection, labeling and packaging of parenteral drugs. You will review batch records, release materials, and ensure documentation compliance throughout finishing operations.

Key requirements include 1–2 years of related experience or equivalent GMP exposure, and proficiency with Word, Excel and Outlook.

Qualifications

• 1–2 years related work experience or equivalent GMP exposure.
• Knowledge of QA principles in pharma/biopharma manufacturing.
• Proficient with Word, Excel and Outlook.
• Bachelor's degree preferred; equivalent GMP experience considered.

Responsibilities

• Verify terminal sterilization, visual inspection, labeling and packaging documentation.
• Review batch records and associated controlled documents.
• Perform QA review and approval of stability and finished product testing certificates.
• Release material and support deviations investigation teams (NCRs/LIRs).

Skills

QA oversight

cGMP knowledge

Microsoft Word

Microsoft Excel

Outlook

Education

Bachelor's degree in Life Sciences or related field

Tools

MS Office Suite

Job description

Grand River Aseptic Manufacturing (GRAM) is seeking a QA Specialist I in Finishing Operations to support cGMP quality systems for terminal sterilization, visual inspection, labeling and packaging of parenteral drugs. You will review batch records, release materials, and ensure documentation compliance throughout finishing operations.

Key requirements include 1–2 years of related experience or equivalent GMP exposure, and proficiency with Word, Excel and Outlook.