QA Specialist – Finishing & Compliance (Pharma)

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

Benefits offered by this job

Health benefits

401(k) plan

Paid volunteer time

PTO

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing Inc. in Grand Rapids, MI, is seeking a QA Specialist I in Finishing Operations to support quality systems for the manufacturing and testing of parenteral products.

The role provides QA oversight for terminal sterilization, visual inspection, labeling and packaging, and reviews documentation for quality release of incoming materials. Non-negotiable requirements include 1-2 years of related experience, GMP knowledge, and proficiency with Word, Excel and Outlook; a

Qualifications

• 1-2 years related work experience.
• GMP/pharma industry knowledge or equivalent experience.
• Proficient with MS Word, Excel, and Outlook.

Responsibilities

• Verify terminal sterilization, visual inspection, labeling and packaging docs.
• Review batch records and controlled documents.
• Perform QA review of stability and finished product test certificates.
• Release incoming materials through QA review.
• Participate in deviation investigations and quality investigations.
• Adhere to cGMPs and company SOPs in daily tasks.

Skills

QA principles

Microsoft Word

Microsoft Excel

Microsoft Outlook

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Grand River Aseptic Manufacturing Inc. in Grand Rapids, MI, is seeking a QA Specialist I in Finishing Operations to support quality systems for the manufacturing and testing of parenteral products.

The role provides QA oversight for terminal sterilization, visual inspection, labeling and packaging, and reviews documentation for quality release of incoming materials. Non-negotiable requirements include 1-2 years of related experience, GMP knowledge, and proficiency with Word, Excel and Outlook; a