QA Specialist - Pharma Quality & Compliance (Day 1 Benefits)

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, prescription, dental, vision

Life insurance

Disability benefits

401(k) with company contributions

Paid volunteer time

PTO and wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing (GRAM) is seeking a Quality Assurance Specialist to support cGMP drug product manufacturing and testing. You will oversee manufacturing documentation, deviations and CAPA, and batch records while supporting the Quality Management System.

Non-negotiable requirements include a Life Sciences degree and 2–5 years of related experience, plus strong computer skills. The role offers comprehensive benefits and growth in a fast-paced, compliant environment.

Qualifications

• Bachelor's degree in Life Sciences or related field; 2–5 years of related work experience, or equivalent GMP experience.
• Must perform tasks with accuracy and efficiency.
• Proficient with Word, Excel and Outlook.

Responsibilities

• Provide on the floor quality oversight within warehouse and manufacturing areas to support SOPs and documentation.
• Establish and maintain proper gowning and cleanroom technique in classified areas.
• Review and approve batch records and other controlled documents.
• Perform QA review of in-process results, environmental monitoring, and material release for incoming materials.
• Participate in cross-functional teams to support quality investigations.
• Understand the relationship between deviations and CAPA within quality systems.

Skills

Attention to detail

Documentation skills

GMP knowledge

Team collaboration

Problem solving

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) is seeking a Quality Assurance Specialist to support cGMP drug product manufacturing and testing. You will oversee manufacturing documentation, deviations and CAPA, and batch records while supporting the Quality Management System.

Non-negotiable requirements include a Life Sciences degree and 2–5 years of related experience, plus strong computer skills. The role offers comprehensive benefits and growth in a fast-paced, compliant environment.