Biopharma Inspector - Visual QA & Packaging (FDA/CGMP)

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical benefits from day 1

Paid volunteer time

Paid time off (PTO) up to 17 days/year

Wellness time off (WTO) per quarter

Paid holidays (10/year)

Shift differential for 2nd/3rd shift

Job summary

Grand River Aseptic Manufacturing (GRAM) in Michigan is seeking a Biopharmaceutical Inspector to ensure the quality and compliance of sterile liquid medications. You will perform visual inspections, assist with labeling and packaging, and follow cGMP procedures under FDA oversight within Finishing.

Non-negotiable: High School Diploma/GED, proficiency in Word/Excel/Outlook, and ability to pass vision screening.

Qualifications

• High School Diploma or GED required.
• Associate degree or equivalent preferred.
• Familiarity with QA, GMP and FDA guidelines is desirable.
• Experience in FDA-regulated pharma environment is a plus.

Responsibilities

• Inspect and label finished products (sterile liquid medicine) per procedures.
• Operate finishing equipment and follow PDA guidelines.
• Document data and complete paperwork accurately.
• Maintain FDA-compliant finishing area and processes.
• Contribute to overall finishing department success.

Skills

QA principles

FDA guidelines

Attention to detail

Education

High School Diploma/GED

Associate degree or equivalent

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) in Michigan is seeking a Biopharmaceutical Inspector to ensure the quality and compliance of sterile liquid medications. You will perform visual inspections, assist with labeling and packaging, and follow cGMP procedures under FDA oversight within Finishing.

Non-negotiable: High School Diploma/GED, proficiency in Word/Excel/Outlook, and ability to pass vision screening.