QA Supervisor: Aseptic Manufacturing & Quality Leadership

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

Benefits offered by this job

Benefits day 1

Paid volunteerism

PTO

Wellness time off

Paid holidays

401(k)

Job summary

Grand River Aseptic Manufacturing (GRAM) seeks a QA Supervisor to lead Quality Systems overseeing Finishing Operations, including inspection, labeling, and packaging. The role collaborates with Operations, Technical Services, Validation, QC, Business and Finance teams to ensure compliance and continuous improvement.

The ideal candidate has a Life Sciences background, 4+ years in QA, and strong knowledge of cGMP, FDA guidelines, and regulatory standards.

Qualifications

• Bachelor’s degree in Life Sciences or related field; or 4+ years of related experience.
• 3+ years in a QA Specialist role.
• Thorough understanding of cGMP and FDA guidelines.

Responsibilities

• Supervise Quality Specialists and Technicians across shifts.
• Oversee Finishing operations and batch release processes.
• Review and approve cGMP documentation and risk assessments.
• Provide client support and interact with auditors/regulators.
• Collaborate with Operations, Technical Services, QC, and Finance teams.

Skills

Leadership

Regulatory knowledge

cGMP expertise

Attention to detail

Education

Bachelor’s degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) seeks a QA Supervisor to lead Quality Systems overseeing Finishing Operations, including inspection, labeling, and packaging. The role collaborates with Operations, Technical Services, Validation, QC, Business and Finance teams to ensure compliance and continuous improvement.

The ideal candidate has a Life Sciences background, 4+ years in QA, and strong knowledge of cGMP, FDA guidelines, and regulatory standards.