QA Technician I – Precision Pharma QA Inspector

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

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism starting day 1

PTO 13 days/year

Wellness time off

Paid holidays

Salary discussed during interview

Job summary

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids seeks a Quality Assurance Technician to perform AQL inspections after visual inspection and packaging steps, and to conduct retention reviews and document assessments.

The role requires attention to accuracy, the ability to work with manufacturing to prioritize inspections, and familiarity with GMP documentation. Full-time on-site position with medical benefits and paid time off.

Qualifications

• High school diploma or equivalent is required.
• Ability to complete tasks with accuracy and efficiency.
• Passing of post-offer vision screening.
• Proficient computer skills in Microsoft Word, Excel, and Outlook.

Responsibilities

• Perform the incoming component and finishing operation AQL inspections (visual inspection, product labeling and/or packaging).
• Communicate effectively with manufacturing to prioritize AQL inspections.
• Uphold procedures and processes for AQL.
• Perform monthly logbook reviews.
• Perform routine current Good Manufacturing Practice reviews on documentation (inventory cards, logbooks etc.).
• Sample finished product for retention and perform monthly retention inspection.
• Provide input into supplier quality investigation reports, corrective actions/preventative actions, customer complaints, and deviation investigations from the visual inspection aspect.

Skills

Quality Assurance

Visual Inspection

Education

High School Diploma or Equivalent

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids seeks a Quality Assurance Technician to perform AQL inspections after visual inspection and packaging steps, and to conduct retention reviews and document assessments.

The role requires attention to accuracy, the ability to work with manufacturing to prioritize inspections, and familiarity with GMP documentation. Full-time on-site position with medical benefits and paid time off.